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21 results for “Pimenta”
Mundo Acadêmico interviews Prof. Marcio Pimenta, CAPES Deputy Coordinator for Administration.
<p><span>What are technical-technological products (TTPs)? How relevant are these products to the impact of academic, professional master's, and doctoral degrees in Brazil? How do the areas of Administration, Accounting and Tourism evaluate these products? To answer these and other questions related to TTPs, Mundo Acadêmico has the honor of interviewing the Deputy Coordinator at CAPES of the Professional Postgraduate Programs in the area of Public and Business Administration, Accounting Sciences, and Tourism, Prof. Dr. Márcio Pimenta. In the conversation, Professor Márcio also details the importance of TTPs in academic programs, giving tips on how to report such products in the quadrennial report, among other unmissable information for students, professors, and coordinators of PPGs linked to Administration, Accounting and Tourism. </span></p> <p>----</p> <p>Contact Prof. Dr. Marcio Pimenta</p> <p>E-mail: 27.admi@capes.gov.br</p> <p><span>----</span></p> <p><span>Documents cited in the interview: </span></p> <p><span>1) Area evaluation form: </span></p> <p><span>https://www.gov.br/capes/pt-br/centrais-de-conteudo/documentos/avaliacao/FICHA_ADMINISTRACAO_P_ATUALIZADA.pdf</span></p> <p><span> </span></p> <p><span>2) DAV Technical Reports and Working Groups: </span></p> <p><span>https://www.gov.br/capes/pt-br/acesso-a-informacao/acoes-e-programas/avaliacao/relatorios-tecnicos-e-grupos-de-trabalho</span></p> <p>----</p>
Distribution. SW Amazonian Brazil (Rondonia State), known only from José Bonifacio Indian Village (12° 10" S and 60° 09' W), where initially collected in 1914, and Pimenta Bueno (12° 12' S and 60° 41° W). in Ctenomyidae
Distribution. SW Amazonian Brazil (Rondonia State), known only from José Bonifacio Indian Village (12° 10" S and 60° 09' W), where initially collected in 1914, and Pimenta Bueno (12° 12' S and 60° 41° W).
FIGURE 3. A in Vocalizations, tadpole, and natural history of Crossodactylus werneri Pimenta, Cruz & Caramaschi, 2014 (Anura: Hylodidae), with comments on distribution and intraspecific variation
FIGURE 3. A density plot of the first discriminant axis (DAPC) on morphological traits from adult males of Crossodactylus werneri. Note the low discrimination among topotypes (blue) and specimens from Serra das Cabras (red). Six principal component axes were retained and explained 95% of total variance.
FIGURE 5 in Vocalizations, tadpole, and natural history of Crossodactylus werneri Pimenta, Cruz & Caramaschi, 2014 (Anura: Hylodidae), with comments on distribution and intraspecific variation
FIGURE 5. Geographic distribution of Crossodactylus werneri in southeastern Brazil. Red circle: type locality (Itatiaia, between the limits of the Brazilian states of Rio de Janeiro, São Paulo, and Minas Gerais); white circles: localities reported by Pimenta et al. (2014); white triangles: new records (present study) from Mococa (above), and Serra das Cabras (Campinas) and Valinhos (below).
FIGURE 4 in Vocalizations, tadpole, and natural history of Crossodactylus werneri Pimenta, Cruz & Caramaschi, 2014 (Anura: Hylodidae), with comments on distribution and intraspecific variation
FIGURE 4. The tadpole (stage 31) of Crossodactylus werneri. From top to bottom: lateral view; dorsal and ventral views of body; oral disc (bottom right). Specimen from Serra das Cabras, Campinas, São Paulo (lot AAG-UFU 5236).
FIGURE 2 in Vocalizations, tadpole, and natural history of Crossodactylus werneri Pimenta, Cruz & Caramaschi, 2014 (Anura: Hylodidae), with comments on distribution and intraspecific variation
FIGURE 2. (A) Adult male specimens of Crossodactylus werneri in life from Serra das Cabras, Campinas, São Paulo: above— AAG-UFU 0981, SVL 21.7 mm; below—AAG-UFU 0982, SVL 21.6 mm. (B) Adult males of Crossodactylus werneri in dorsal view. Left—Serra das Cabras, Campinas, São Paulo (AAG-UFU 1880; SVL 23.0 mm); right—Parque Nacional do Itatiaia, Rio de Janeiro (topotype ZUEC-AMP 7981; SVL 22.1 mm). (C) Adult males of Crossodactylus werneri from Serra das Cabras (Campinas, São Paulo), depicting variation in size and in the degree of reticulation on the belly (right—AAG-UFU 1875, SVL 21.6 mm; left—AAG-UFU 1878, SVL 25.1 mm).
FIGURE 1 in Vocalizations, tadpole, and natural history of Crossodactylus werneri Pimenta, Cruz & Caramaschi, 2014 (Anura: Hylodidae), with comments on distribution and intraspecific variation
FIGURE 1. (A) From top to bottom: oscillogram of a 29-note advertisement call of Crossodactylus werneri preceded by five isolated notes (second note identified by a red arrow); spectrogram of three median notes and respective oscillogram. Sound file: Crossod_werneriSousasSP1aAAGm671. (B) Spectrogram and respective oscillogram of the territorial call of Crossodactylus werneri. Sound file: Crossod_werneriSousasSP1eAAGm671. Further information on these recordings is provided in Appendix III.
FIGURE 2. A–E Pimenta dioica. A in Revisiting the identity and distribution of Allspice (Myrtaceae), a misidentified spice in India
FIGURE 2. A–E Pimenta dioica. A—Trunk, B—inflorescence, C—flower with 4 lobed corolla, D—fruit bunch, E—split fruit with seed. F–J Pimenta racemosa. F—Trunk, G—inflorescence, H—flower with 5 lobed corolla, I—fruit bunch, J—seed.
FIGURE 64. Syagrus pimentae. A. Habit. B. Palm with Ricardo Pimenta for scale. C. Palm showing Butia-like leaves with evenly spaced leaflets. D. Old inflorescences. E. Newly opened inflorescence. F. Infructescence. G in A revision of the genus Syagrus (Arecaceae)
FIGURE 64. Syagrus pimentae. A. Habit. B. Palm with Ricardo Pimenta for scale. C. Palm showing Butia-like leaves with evenly spaced leaflets. D. Old inflorescences. E. Newly opened inflorescence. F. Infructescence. G. Whole plant with infructescence. (Pimenta & Campos-Rocha s.n. [holotype HPL]).
FIGURE 2 in One new species, two new combinations and taxonomic notes on the All-spice genus Pimenta (Myrtaceae) from Hispaniola
FIGURE 2. Field pictures and details of Pimenta berciliae (A–H). (A) Fertile branch with subterminal inflorescence; (B) Leaves with slightly revolute margins; (C) Reddish brown bark, somewhat papery-flaky; (D) Adaxial and (E) abaxial leaf surfaces, showing color difference between surfaces in fresh material. (F) 3-flowered inflorescence with slightly assymetrical lateral branching; (G) Old flower with stamens only partially present showing reflexed petals; (H) Frontal view of old flower remains (without stamens or petals) showing the five calyx lobes and the pentagonous hypanthium.
FIGURE 1 in One new species, two new combinations and taxonomic notes on the All-spice genus Pimenta (Myrtaceae) from Hispaniola
FIGURE 1. Distribution and phylogenetic position of treated species within Pimenta. (A) Natural distributions of Pimenta berciliae (red circles); P. yumana (yellow triangle) and P. samanensis (yellow star). (B) An extract from the Myrteae phylogeny (see Vasconcelos et al., 2017 for methodology) based on maximum likelihood analysis of two markers (ITS and psbA-trnH; see Appendix 1 for Genbank accession codes) showing phylogenetic positions of Pimenta berciliae and Pimenta yumana. Bootstrap values above 90 are given at each node.
Figure 1 from: de Souza LS, Pimenta AD (2019) Eulimacrostoma gen. nov., a new genus of Eulimidae (Gastropoda, Caenogastropoda) with description of a new species and reevaluation of other western Atlantic species. Zoosystematics and Evolution 95(2): 403-415. https://doi.org/10.3897/zse.95.33880
Figure 1 - Eulimacrostoma microsculpturata gen. nov. and sp. nov. A. Holotype (USNM 429762); B, C. Paratype (USNM 433081); D–G. Paratype (FLMNH uncatalogued.) A, B, D. Shell in frontal view; C, E. Shell in lateral view; F. Detail of apical whorls in frontal view; G. Specimen attached to the host Luidia ludwigi scotti Bell, 1917 (Echinoderm collection, FLMNH 5042), red ellipse indicates the eulimid. Scale bars: 1 mm (A–E); 100 µm (F).
Figure 2 from: de Souza LS, Pimenta AD (2019) Eulimacrostoma gen. nov., a new genus of Eulimidae (Gastropoda, Caenogastropoda) with description of a new species and reevaluation of other western Atlantic species. Zoosystematics and Evolution 95(2): 403-415. https://doi.org/10.3897/zse.95.33880
Figure 2 - Eulimacrostoma microsculpturata gen. nov. and sp. nov. A–E. Paratype (ANSP 312431); F. Paratype (USNM 433081); G. Paratype (USNM 417511). A, C. whole shell in ventral view; B. Shell in lateral view; D. Detail of body whorl in frontal view; E. Detail of teleoconch surface, white arrows indicates the microsculpture of axial lines; F. Detail of apical whorls in frontal view; G. Detail of protoconch in apical view, white arrow indicates the transition protoconch-teleoconch. Scale bars: 1 mm (A–C); 500 µm D); 100 µm (E, G); 200 µm (F).
Figure 5 from: de Souza LS, Pimenta AD (2019) Eulimacrostoma gen. nov., a new genus of Eulimidae (Gastropoda, Caenogastropoda) with description of a new species and reevaluation of other western Atlantic species. Zoosystematics and Evolution 95(2): 403-415. https://doi.org/10.3897/zse.95.33880
Figure 5 - Geographical distributions of Eulimacrostoma spp. based on confirmed identifications. A. Eulimacrostoma microsculpturata sp. nov.; B. Eulimacrostoma chascanon (Watson, 1883), comb. nov.; C. Eulimacrostoma fusus (Dall, 1889), comb. nov.; D. Eulimacrostoma lutescens (Simone, 2002), comb. nov.; E. Eulimacrostoma patula (Dall & Simpson, 1901), comb. nov. White circle: type locality; black circle: additional records. Records without geographic coordinates are approximate.
Figure 3 from: de Souza LS, Pimenta AD (2019) Eulimacrostoma gen. nov., a new genus of Eulimidae (Gastropoda, Caenogastropoda) with description of a new species and reevaluation of other western Atlantic species. Zoosystematics and Evolution 95(2): 403-415. https://doi.org/10.3897/zse.95.33880
Figure 3 - Eulimacrostoma spp. A–C. Eulimacrostoma chascanon (Watson, 1883), comb. nov.: A, B. Lectotype herein designated (NHMUK 1887.2.9.1587); C. Paralectotype (NHMUK Norman Coll. 1979225); D–I. Eulimacrostoma fusus (Dall, 1889), comb. nov.: D, E, G–I. Lectotype herein designated (USNM 87273); G. Paralectotype (MCZ 7515). J–N. Eulimacrostoma lutescens (Simone, 2002), comb. nov.: J, K. Holotype (MNHN-IM 2000-5662); L–N. (MNHN-IM uncatalogued), from type locality. A, C–E, G, K, M. Shell in frontal view; B. Shell in dorsal view; F, L, N. Shell in lateral view; H, O. Detail of apical whorls in frontal view; I, J. Detail of teleoconch surface, white square in I indicates detail in J, white arrows in J indicates microsculpture of axial lines. Scale bars: 1 mm (A–G, I, K–N); 400 µm (H); 50 µm (J); 200 µm (O). Credits: A–C: NHMUK; H, I: USNM; J, K: MNHN-IM.
Figure 4 from: de Souza LS, Pimenta AD (2019) Eulimacrostoma gen. nov., a new genus of Eulimidae (Gastropoda, Caenogastropoda) with description of a new species and reevaluation of other western Atlantic species. Zoosystematics and Evolution 95(2): 403-415. https://doi.org/10.3897/zse.95.33880
Figure 4 - Eulimacrostoma patula (Dall & Simpson, 1901), comb. nov. A. Lectotype herein designated (USNM 160202); B, F. (MCZ 34479); C. (MCZ 34476). D–E, G–K. (MCZ 34589). A–D. Shell in frontal view; E. Shell in lateral view; F. Detail of teleoconch surface, white arrows indicates microsculpture of axial lines; G. Detail of body whorl in ventral view; H. detail of body whorl in lateral view; I. Detail of umbilical fissure; J. Detail of apical whorls in frontal view; K. Detail of protoconch in apical view, white arrow indicates the transition from protoconch to teleoconch. Scale bars: 1 mm (A–E); 200 µm (F–H); 100 µm (I–K). Credits: A: USNM.
FIGURE 3 in One new species, two new combinations and taxonomic notes on the All-spice genus Pimenta (Myrtaceae) from Hispaniola
FIGURE 3. Isotype image of Pimenta berciliae at K.
Figure 4 from: Pimenta A, Santos F, Cunha C (2018) Reassignment of Acteon semicingulatus to the Pyramidellidae, with review of the occurrence of Ondina and Evalea in the Western Atlantic (Gastropoda). Zoosystematics and Evolution 94(2): 1-10. https://doi.org/10.3897/zse.94.28765
Figure 4 A. Shell of Odostomiafernandina, holotype (USNM 108053) in apertural view; B. same, in adapertural view. Scale bar: 1 mm.
Figure 1 from: Pimenta A, Santos F, Cunha C (2018) Reassignment of Acteon semicingulatus to the Pyramidellidae, with review of the occurrence of Ondina and Evalea in the Western Atlantic (Gastropoda). Zoosystematics and Evolution 94(2): 1-10. https://doi.org/10.3897/zse.94.28765
Figure 1 Shells of Ondinasemicingulata. A. Syntype (USNM 107913), in apertural view; B. same in lateral view; C. same in ventral view; D. same, detail of protoconch in apical view. E. From Rio Grande do Norte state (MNRJ 27821), in apertural view; F. same, lateral view; G. same, adapertural view; H. same, detail of protoconch in apical view; I. same, detail of sculpture. J. From Brazil, Amapá state (MNRJ 27809), shell #1 in apertural view; K. same, shell #2 in ventral view. L. From Brazil, Bahia state, MNRJ 28264, in apertural view. M. From Brazil, Amapá state (MNRJ 26217), in ventral view. N. From Brazil, Rio Grande do Norte state (MNRJ 27834), in apertural view. Scale bars: whole shells (vertical bar): 1 mm; details (horizontal bar): 200 µm.
Figure 3 from: Pimenta A, Santos F, Cunha C (2018) Reassignment of Acteon semicingulatus to the Pyramidellidae, with review of the occurrence of Ondina and Evalea in the Western Atlantic (Gastropoda). Zoosystematics and Evolution 94(2): 1-10. https://doi.org/10.3897/zse.94.28765
Figure 3 A. Shell of Ondinahendersoni, holotype (USNM 203813) in apertural view; B. same, in lateral view. C. Shell of Ondinastocki, holotype (ZMA.MOLL. 138319) in apertural view [photo: Naturalis, Jeroen Goud. D.Ondinastocki, paratype (ZMA.MOLL. 138320), smaller shell in apertural view; E. same, bigger shell in apertural view. Scale bar: 1 mm.
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