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686 results for “Lima”

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zenodo28/100

Figures 15-18 from: De Assis JE, Souza JRB, Lima MM, Lima GV, Cordeiro RTS, Pérez CD (2019) Association between deep-water scale-worms (Annelida: Polynoidae) and black corals (Cnidaria: Antipatharia) in the Southwestern Atlantic. Zoologia 36: 1-13. https://doi.org/10.3897/zoologia.36.e28714

Figures 15-18 (15) Head of P.cf.greeffi showing the prostomium and their structures; (16) Parapodia of P.cf.greeffi showing notochaetae and neurochaetae; (17) Neurochaetae from median chaetigers of P.cf.greeffi; (18) Detail of distal tip of neurochaetae. (ch) Chaetae, (cp) cephalic peak, (la) lateral antennae, (ma) median antennae, (ng) nuchal groove, (pl) palp, (pr) prostomium. Scale bars: 15 = 1 mm, 16–17 = 100 µm, 18 = 10 µm.

opencc-by-4.0Jun 2019View details →
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Figures 19-21 from: De Assis JE, Souza JRB, Lima MM, Lima GV, Cordeiro RTS, Pérez CD (2019) Association between deep-water scale-worms (Annelida: Polynoidae) and black corals (Cnidaria: Antipatharia) in the Southwestern Atlantic. Zoologia 36: 1-13. https://doi.org/10.3897/zoologia.36.e28714

Figures 19-21 (19) Corallum morphology of Tanacetipathestanacetum; (20) cross section showing pinnules cycle of T.tanacetum; (21) organization of spines in T.tanacetum. Sacale bars: 19, 20 = 1 cm, 21 = 200 μm.

opencc-by-4.0Jun 2019View details →
zenodo28/100

Figure 1 from: De Assis JE, Souza JRB, Lima MM, Lima GV, Cordeiro RTS, Pérez CD (2019) Association between deep-water scale-worms (Annelida: Polynoidae) and black corals (Cnidaria: Antipatharia) in the Southwestern Atlantic. Zoologia 36: 1-13. https://doi.org/10.3897/zoologia.36.e28714

Figure 1 Records of association of scale-worm polynoids and black corals from deep-water in South America, Northeastern Brazil: (A) record of Benhamypolynoecf.antipathicola, and its antipatharian hosts Stylopathesadinocrada in Potiguar Basin; (B) records of association of Parahololepidellacf.greeffi and its antipatharian hosts (Tanacetipathesbarbadensis, T.tanacetum and T.thamnea) in Potiguar Basin, Brazil.

opencc-by-4.0Jun 2019View details →
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Figures 11-14 from: De Assis JE, Souza JRB, Lima MM, Lima GV, Cordeiro RTS, Pérez CD (2019) Association between deep-water scale-worms (Annelida: Polynoidae) and black corals (Cnidaria: Antipatharia) in the Southwestern Atlantic. Zoologia 36: 1-13. https://doi.org/10.3897/zoologia.36.e28714

Figures 11-14 (11) Parahololepidellacf.greeffi on the branches of Tanacetipathestanacetum; (12) median chaetigers of P.greeffi showing elytra and dorsal cirri; (13) head of P.greeffi showing the prostomium, palps and antennae; (14) elytrae from posterior chaetigers of P.cf.greeffi showing a smooth edge. (cp) Cephalic peak, (dc) dorsal cirrus, (el) elytra, (et) elythophore, (la) lateral antennae, (ma) median antennae, (pa) parapodium, (pl) palp, (pr) prostomium, (tc) tentacular cirrus. Scale bars: 11–13 = 1 mm, 14 = 100 µm.

opencc-by-4.0Jun 2019View details →
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Figures 22-27 from: De Assis JE, Souza JRB, Lima MM, Lima GV, Cordeiro RTS, Pérez CD (2019) Association between deep-water scale-worms (Annelida: Polynoidae) and black corals (Cnidaria: Antipatharia) in the Southwestern Atlantic. Zoologia 36: 1-13. https://doi.org/10.3897/zoologia.36.e28714

Figures 22-27 (22) Corallum morphology of Tanacetipathesbarbadensis; (23) cross section showing pinnules cycle of T.barbadensis; (24) organization of spines in T.barbadensis; (25) corallum morphology of Tanacetipathesthamnea; (26) cross section showing pinnules cycle of T.thamnea; (27) organization of spines in T.thamnea. Scale bars: 22, 23, 25, 26 = 1 cm, 24 = 200 μm, 27 = 150 μm.

opencc-by-4.0Jun 2019View details →
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Supplementary material 2 from: Nobile AB, Freitas-Souza D, Ruiz-Ruano FJ, Nobile MLMO, Costa GO, de Lima FP, Camacho JPM, Foresti F, Oliveira C (2019) DNA metabarcoding of Neotropical ichthyoplankton: Enabling high accuracy with lower cost. Metabarcoding and Metagenomics 3: e35060. https://doi.org/10.3897/mbmg.3.35060

: Data type: NGS quality control

opencc-zeroSep 2019View details →
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Supplementary material 1 from: Nobile AB, Freitas-Souza D, Ruiz-Ruano FJ, Nobile MLMO, Costa GO, de Lima FP, Camacho JPM, Foresti F, Oliveira C (2019) DNA metabarcoding of Neotropical ichthyoplankton: Enabling high accuracy with lower cost. Metabarcoding and Metagenomics 3: e35060. https://doi.org/10.3897/mbmg.3.35060

: Data type: Bioinformatic protocol

opencc-zeroSep 2019View details →
zenodo28/100

Linked collectors and determiners for: IPA - Herbário - IPA Dárdano de Andrade Lima.

Natural history specimen data linked to collectors and determiners held within, "IPA - Herbário - IPA Dárdano de Andrade Lima". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/f45c5ee0-e5ec-42e3-a80a-07318144efa4">https://bionomia.net/dataset/f45c5ee0-e5ec-42e3-a80a-07318144efa4</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/f45c5ee0-e5ec-42e3-a80a-07318144efa4">https://gbif.org/dataset/f45c5ee0-e5ec-42e3-a80a-07318144efa4</a>. Formatted as a Frictionless Data package.

opencc-zeroJan 2024View details →
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Linked collectors and determiners for: HCDAL - Herbário Caririense Dárdano de Andrade-Lima.

Natural history specimen data linked to collectors and determiners held within, "HCDAL - Herbário Caririense Dárdano de Andrade-Lima". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/aed35888-68cb-4574-8a98-d13b89cf0f38">https://bionomia.net/dataset/aed35888-68cb-4574-8a98-d13b89cf0f38</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/aed35888-68cb-4574-8a98-d13b89cf0f38">https://gbif.org/dataset/aed35888-68cb-4574-8a98-d13b89cf0f38</a>. Formatted as a Frictionless Data package.

opencc-zeroJan 2024View details →
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Linked collectors and determiners for: First record in Colombia of Microscapus hymenaeae Costa Lima, 1950 (Coleoptera: Curculionidae: Cryptorhynchini).

Natural history specimen data linked to collectors and determiners held within, "First record in Colombia of Microscapus hymenaeae Costa Lima, 1950 (Coleoptera: Curculionidae: Cryptorhynchini)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/9ef1646d-d8cb-40fd-85c3-6b3e0ae6ff68">https://bionomia.net/dataset/9ef1646d-d8cb-40fd-85c3-6b3e0ae6ff68</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/9ef1646d-d8cb-40fd-85c3-6b3e0ae6ff68">https://gbif.org/dataset/9ef1646d-d8cb-40fd-85c3-6b3e0ae6ff68</a>. Formatted as a Frictionless Data package.

opencc-zeroOct 2024View details →
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Fig. 24 in Morphology of the Braincase in the Cretaceous Hybodont Shark Tribodus limae (Chondrichthyes: Elasmobranchii), Based on CT Scanning

Fig. 24. Close-up of lateral basicranial foramina in Tribodus limae (UERJ-PMB-40). Scale bar is 1 cm.

opencc-by-4.0Mar 2010View details →
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Fig. 7 in Morphology of the Braincase in the Cretaceous Hybodont Shark Tribodus limae (Chondrichthyes: Elasmobranchii), Based on CT Scanning

Fig. 7. Transverse CT scan slices through the Tribodus limae braincase. Orbital region. A, slice 187, at the level of the optic nerve; B, slice 209, at the level of the oculomotor nerve; C, slice 216, at the level of the oculomotor nerve showing the anterior semicircular canal originating anterior to the postorbital process; D, E, slices 222 and 226, respectively, at the level of the efferent pseudobranchial foramen and the foramen for the superficial ophthalmic complex and profundus nerve; F, slice 239, at the level of the utricular recess and abducens foramen; G, H, slices 241 and 242, respectively, showing the course of the superficial ophthalmic complex and abducens nerve within the cartilage of the orbit. No scale.

opencc-by-4.0Mar 2010View details →
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Figure 3 from: Majure L, Bécquer E, Judd W (2014) Miconia bullotricha and M. hirtistyla, two new species of Miconia sect. Lima (Miconieae, Melastomataceae) from eastern Cuba. PhytoKeys 33: 61-75. https://doi.org/10.3897/phytokeys.33.6766

Figure 3 - Illustration of Miconia hirtistyla. A habit (Ekman 14617) B leaf abaxial surface (León LS-10923) C bracteole (León LS-10923) D petal (Ekman 14617) E stamen (Ekman 14617) F style (Ekman 14617).

opencc-by-4.0Jan 2014View details →
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Figure 4 from: Majure L, Bécquer E, Judd W (2014) Miconia bullotricha and M. hirtistyla, two new species of Miconia sect. Lima (Miconieae, Melastomataceae) from eastern Cuba. PhytoKeys 33: 61-75. https://doi.org/10.3897/phytokeys.33.6766

Figure 4 - Illustration of Miconia jashaferi. A habit (Ekman 3849) B petal (Alain 871) C stamen (Alain 871) D style (Alain 871) E immature fruit longitudinal section (Alain 871), seed (Acuña SV-13275).

opencc-by-4.0Jan 2014View details →
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Figure 2 from: Majure L, Bécquer E, Judd W (2014) Miconia bullotricha and M. hirtistyla, two new species of Miconia sect. Lima (Miconieae, Melastomataceae) from eastern Cuba. PhytoKeys 33: 61-75. https://doi.org/10.3897/phytokeys.33.6766

Figure 2 - Distribution of Miconia hirtistyla in Granma and Santiago de Cuba provinces (closed circles) and Miconia bullotricha in Guantánamo Province (open circles).

opencc-by-4.0Jan 2014View details →
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Figure 1 from: Majure L, Bécquer E, Judd W (2014) Miconia bullotricha and M. hirtistyla, two new species of Miconia sect. Lima (Miconieae, Melastomataceae) from eastern Cuba. PhytoKeys 33: 61-75. https://doi.org/10.3897/phytokeys.33.6766

Figure 1 - Illustration of Miconia bullotricha. A habit B close-up of leaf adaxial surface C immature stamen D style E fruit longitudinal section F seed (all from Bisse et al. HFC-49930).

opencc-by-4.0Jan 2014View details →
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Figure 8 from: K. Klishko O, Lopes-Lima M, Froufe E, Bogan A (2014) Are Cristaria herculea (Middendorff, 1847) and Cristaria plicata (Leach, 1815) (Bivalvia, Unionidae) separate species? ZooKeys 438: 1-15. https://doi.org/10.3897/zookeys.438.7493

Figure 8 - Phylogenetic tree obtained by Bayesian Inference and Maximum Likelihood analyses, using mtDNA fragments (CO1). Support values are given as Bayesian posterior probability above nodes and as bootstrap support below nodes, except for those within major clades, which have been omitted for clarity. Available sequences downloaded from GenBank and new sequences codes refer to Table 2.

opencc-by-4.0Aug 2014View details →
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Figure 5 from: K. Klishko O, Lopes-Lima M, Froufe E, Bogan A (2014) Are Cristaria herculea (Middendorff, 1847) and Cristaria plicata (Leach, 1815) (Bivalvia, Unionidae) separate species? ZooKeys 438: 1-15. https://doi.org/10.3897/zookeys.438.7493

Figure 5 - Cristaria herculea: A excurrent aperture (to the left) and incurrent aperture (to the right) B excurrent aperture (magnification) C shape of papillae in incurrent aperture (magnification).

opencc-by-4.0Aug 2014View details →
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Figure 4 from: K. Klishko O, Lopes-Lima M, Froufe E, Bogan A (2014) Are Cristaria herculea (Middendorff, 1847) and Cristaria plicata (Leach, 1815) (Bivalvia, Unionidae) separate species? ZooKeys 438: 1-15. https://doi.org/10.3897/zookeys.438.7493

Figure 4 - Morphology of Cristaria herculea soft body: a – mantle, b – outer gill, c – inner gill, d – foot, e – labial palps, f – incurrent aperture, g – excurrent aperture, h – supra-anal aperture, i – dorsal adductor muscle, j – mantle bridge, k – dorsal wing mantle projections, l – muscular anterior margin of dorsal mantle wing.

opencc-by-4.0Aug 2014View details →
zenodo28/100

Figure 1 from: K. Klishko O, Lopes-Lima M, Froufe E, Bogan A (2014) Are Cristaria herculea (Middendorff, 1847) and Cristaria plicata (Leach, 1815) (Bivalvia, Unionidae) separate species? ZooKeys 438: 1-15. https://doi.org/10.3897/zookeys.438.7493

Figure 1 - Cristaria herculea from Upper Amur River basin. A, B from Kharanorsky reservoir C from Buir-Nur Lake (Mongolia) D from Onon River E from Shilka River F from Nercha River. Scale bar 1 cm.

opencc-by-4.0Aug 2014View details →

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