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Supplementary material 1 from: Serafim-Júnior M, Perbiche-Neves G, Lansac-Toha F (2019) Environments and macrophytes as main variables controlling rotifers in a river/lake system before Porto Primavera Reservoir construction. Zoologia 36: 1-8. https://doi.org/10.3897/zoologia.36.e24191
Table S1. List of species found in our study, separated by their habitat (H) occurrence in the pelagic (P) or littoranean (L) region
Distribution. Discontinuous and limited to wetland environments in the Congo Basin N and W of the range of the Zambezi Sitatunga in S Benin (Porto Novo), S Nigeria, Cameroon, Central African Republic, Equatorial Guinea, Gabon, Republic of the Congo, N DR Congo; also several isolated populations in W Africa (Senegal, Gambia & Guinea-Bissau), NE Nigeria and W Chad, and perhaps extreme S Ghana. Maps and distributional information here are provisional pending future research. in Bovidae
Distribution. Discontinuous and limited to wetland environments in the Congo Basin N and W of the range of the Zambezi Sitatunga in S Benin (Porto Novo), S Nigeria, Cameroon, Central African Republic, Equatorial Guinea, Gabon, Republic of the Congo, N DR Congo; also several isolated populations in W Africa (Senegal, Gambia & Guinea-Bissau), NE Nigeria and W Chad, and perhaps extreme S Ghana. Maps and distributional information here are provisional pending future research.
Distribution. Madeira Archipelago (Madeira and Porto Santo) and W Canary Is (La Palma, La Gomera, El Hierro, and Tenerife). Individuals classified as Pipistrellus sp. from the Azores have been suggested to be Madeira Pipistrelles. in Vespertilionidae
Distribution. Madeira Archipelago (Madeira and Porto Santo) and W Canary Is (La Palma, La Gomera, El Hierro, and Tenerife). Individuals classified as Pipistrellus sp. from the Azores have been suggested to be Madeira Pipistrelles.
Distribution. Discontinuous and limited to wetland environments in the Congo Basin N and W of the range of the Zambezi Sitatunga in S Benin (Porto Novo), S Nigeria, Cameroon, Central African Republic, Equatorial Guinea, Gabon, Republic of the Congo, N DR Congo; also several isolated populations in W Africa (Senegal, Gambia & Guinea-Bissau), NE Nigeria and W Chad, and perhaps extreme S Ghana. Maps and distributional information here are provisional pending future research. in Bovidae
Distribution. Discontinuous and limited to wetland environments in the Congo Basin N and W of the range of the Zambezi Sitatunga in S Benin (Porto Novo), S Nigeria, Cameroon, Central African Republic, Equatorial Guinea, Gabon, Republic of the Congo, N DR Congo; also several isolated populations in W Africa (Senegal, Gambia & Guinea-Bissau), NE Nigeria and W Chad, and perhaps extreme S Ghana. Maps and distributional information here are provisional pending future research.
Distribution. Bolivian lowlands (NE to the Chiquitano Mts and SW to the piedmont elevations in the subandean region) and SW Brazilian Amazon in the upper Madeira River, and the Beni, Ichilo, Marmoré, Ipurupuru, Iboré, Baré, Abuna, and Iténez (= Guaporé) rivers and their tributaries, all of which drain into the Madeira; recently also recorded below Santo Antonio falls between the cities of Porto Velho and Borba. in Iniidae
Distribution. Bolivian lowlands (NE to the Chiquitano Mts and SW to the piedmont elevations in the subandean region) and SW Brazilian Amazon in the upper Madeira River, and the Beni, Ichilo, Marmoré, Ipurupuru, Iboré, Baré, Abuna, and Iténez (= Guaporé) rivers and their tributaries, all of which drain into the Madeira; recently also recorded below Santo Antonio falls between the cities of Porto Velho and Borba.
FIGURE. Drosera hirticalyx (a–c): a, habit; b, inflorescence; c, flower (Kukenán-tepui, Venezuela). Drosera intermedia (d–f): d, habit; e, rosette (Porto Seguro, BA); f, inflorescence with open flower (cultivated). Drosera latifolia (g–i): g, rosette (Parque Nacional das Sempre-Vivas, MG); h, rosettes (Mogi das Cruzes, SP); i, flowers (Diamantina, MG). Photo credits: a–c by AF; d, e by FR; f–i by PMG. in A synopsis of the genus Drosera (Droseraceae) in Brazil
FIGURE. Drosera hirticalyx (a–c): a, habit; b, inflorescence; c, flower (Kukenán-tepui, Venezuela). Drosera intermedia (d–f): d, habit; e, rosette (Porto Seguro, BA); f, inflorescence with open flower (cultivated). Drosera latifolia (g–i): g, rosette (Parque Nacional das Sempre-Vivas, MG); h, rosettes (Mogi das Cruzes, SP); i, flowers (Diamantina, MG). Photo credits: a–c by AF; d, e by FR; f–i by PMG.
46: Localização de Falhas de Software, com Rui Maranhão Abreu (Universidade do Porto e Meta)
<p>Este episódio do podcast “Fronteiras da Engenharia de Software” com Rui Maranhão Abreu aborda a localização de falhas de software e suas aplicaçõe. Rui, professor catedrático em Engenharia de Software na Universidade do Porto e Research Software Engineer na Meta, compartilha ideias sobre esse campo da Engenharia de Software.</p> <p>No episódio, são discutidos conceitos fundamentais, como a diferença entre falhas e bugs, bem como os desafios enfrentados na detecção de falhas em sistemas complexos e distribuídos, especialmente em ambientes de integração contínua, como na Meta. Rui também explora o papel da inteligência artificial, machine learning e deep learning na localização de falhas e destaca avanços recentes na pesquisa de reparo automatizado de programas.</p> <p>Além disso, são abordados artigos recentes de Rui e seus co-autores, incluindo o “Remoção de Código Morto na Meta”, que apresenta o Framework de Remoção Sistemática de Código e Ativos (SCARF), e “Depuração de Erros de Tipo Alimentada por GPT-3”, que descreve uma técnica para corrigir automaticamente erros de tipo em programas OCaml, utilizando o GPT-3.</p> <p>A conversa também explora a carreira de Rui na Meta, sua experiência como General Chair do ICSE 2024 em Portugal e suas visões sobre a próxima fronteira da engenharia de software.</p> <p>Site de Rui: <a href="https://ruimaranhao.com/">https://ruimaranhao.com/</a></p> <p>Outros links:</p> <ul> <li> <p><a href="https://sigarra.up.pt/feup/pt/func_geral.formview?p_codigo=466651">https://sigarra.up.pt/feup/pt/func_geral.formview?p_codigo=466651</a></p> </li> <li> <p><a href="https://dei.fe.up.pt/pt/blog/2023/04/10/rui-maranhao-toma-posse-como-diretor-do-prodei/">https://dei.fe.up.pt/pt/blog/2023/04/10/rui-maranhao-toma-posse-como-diretor-do-prodei/</a></p> </li> </ul> <p>Artigos:</p> <p>“Remoção de Código Morto na Meta: Exclusão Automática de Milhões de Linhas de Código e Petabytes de Dados Obsoletos”</p> <p>“Dead Code Removal at Meta: Automatically Deleting Millions of Lines of Code and Petabytes of Deprecated Data”</p> <p><a href="https://dl.acm.org/doi/10.1145/3611643.3613871">https://dl.acm.org/doi/10.1145/3611643.3613871</a></p> <p>Localização de características baseada em espectro: um estudo de caso usando o ArgoUML.</p> <p>Spectrum-based feature localization: a case study using ArgoUML</p> <p><a href="https://dl.acm.org/doi/abs/10.1145/3461001.3473065">https://dl.acm.org/doi/abs/10.1145/3461001.3473065</a></p> <p>Depuração de Erros de Tipo Alimentada por GPT-3: Investigando o Uso de Modelos de Linguagem Avançados para Reparo de Código</p> <p>GPT-3-Powered Type Error Debugging: Investigating the Use of Large Language Models for Code Repair</p> <p><a href="https://dl.acm.org/doi/abs/10.1145/3623476.3623522">https://dl.acm.org/doi/abs/10.1145/3623476.3623522</a> </p> <p>Mentat (ferramenta) <a href="https://figshare.com/articles/software/GPT-3-Powered_Type_Error_Debugging_Investigating_the_Use_of_Large_Language_Models_for_Code_Repair_SLE_2023_/23646903">https://figshare.com/articles/software/GPT-3-Powered_Type_Error_Debugging_Investigating_the_Use_of_Large_Language_Models_for_Code_Repair_SLE_2023_/23646903</a></p> <p>The bumpy road of taking automated debugging to industry</p> <p><a href="https://arxiv.org/abs/2212.01237">https://arxiv.org/abs/2212.01237</a></p> <p>Outros links: </p> <p>ICSE 2024 <a href="https://conf.researchr.org/home/icse-2024">https://conf.researchr.org/home/icse-2024</a></p> <p>FSE 2024 <a href="https://conf.researchr.org/home/fse-2024">https://conf.researchr.org/home/fse-2024</a></p> <p>ICSE 2026 <a href="https://twitter.com/rafaelpri/status/1543318975043383296">https://twitter.com/rafaelpri/status/1543318975043383296</a></p> <p>Mais informações em <a href="https://fronteirases.github.io/episodios/paginas/46">https://fronteirases.github.io/episodios/paginas/46</a></p> <p>Entrevistadores: Adolfo Neto (PPGCA UTFPR) <a href="https://adolfont.github.io/">https://adolfont.github.io</a> e Maria Claudia Emer</p> <p>Nosso site é: <a>https://fronteirases.github.io</a> </p> <p>Extreme Energy (Music Today 80). Composed & Produced by: Anwar Amr. Link: <a href="https://www.youtube.com/watch?v=8ZZbAkKNx7s%E2%81%A0">https://www.youtube.com/watch?v=8ZZbAkKNx7s</a> </p> <p>Data de publicação: 15 de maio de 2024.</p>
FIGURA 1 in Nidificação Colonial De Butorides Striata (Linnaeus, 1758) (Ciconiiformes: Ardeidae) Em Área Alagável No Município De Porto Esperidião, Mato Grosso
FIGURA 1: Número de ninhos ativos em cada período (ovos e ninhegos), em área alagável, município de Porto Esperidião, na estação reprodutiva de 2010.
PLATE 3 in A new species of Pericallis (Senecioneae, Asteraceae) endemic to Porto Santo (Madeira, Portugal)
PLATE 3. Pericallis menezesii (holotype): a, habit; b, adaxial leaf lamina surface; c, involucre bract; d, disc cypsela; e, disc floret; f, longitudinal section of disc floret; g, disc pappus; h, disc floret style apex; i, ray floret; j, ray floret style apex. Pericallis aurita (R. Jardim RJ 3057 (BM)): k, habit; l, abaxial leaf lamina surface; m, base of petiole; n, involucre bract; o, disc cypsela. Drawn by Rosemary Wise (Department of Plant Sciences, University of Oxford).
PLATE 1 in A new species of Pericallis (Senecioneae, Asteraceae) endemic to Porto Santo (Madeira, Portugal)
PLATE 1. Pericallis menezesii: a, habit (Pico Branco, R. Jardim, 16/05/2010); b, capitula (Pico Branco, Miguel Sequeira, 29/04/2013).
FIGURE 73 in New Amphicocconeis (Bacillariophyta) from Raivavae and Tahiti Islands (South Pacific) and Porto Belo (Brazil), with re-examination of Psammococconeis
FIGURE 73. Cladistic analysis of ultrastructural characters. 9 Amphicocconeis (Table 3), 13 characters (Table 2). Cocconeis scutellum Ehrenberg as an outgroup. Majority rule consensus tree resulting from the 12 most parsimonious trees.
FIGURES 66–68 in New Amphicocconeis (Bacillariophyta) from Raivavae and Tahiti Islands (South Pacific) and Porto Belo (Brazil), with re-examination of Psammococconeis
FIGURES 66–68. Amphicocconeis cf. mascarenica. (material from Raivavae, Tahiti and Moorea Isls, South Pacific). RV in internal view, with RVVC still in place, note the regularly biseriate row of alternate round pores corresponding to each RV stria (Fig. 66), RVVC apex in abvalvar side (Fig. 67), complete and open RVVC in advalvar view (Fig. 68). Scale bars: 3 µm (Figs 66, 68), 600 µm (Fig. 67).
FIGURES 55–61 in New Amphicocconeis (Bacillariophyta) from Raivavae and Tahiti Islands (South Pacific) and Porto Belo (Brazil), with re-examination of Psammococconeis
FIGURES 55–61. Amphicocconeis ruatara sp. nov. (material RAI 20 from Raivavae, Austral Islands, South Pacific). RVs in external view (Figs 55–56), RV in internal view (Fig. 57), detail of the RV apex with terminal raphe fissure (Fig. 58), central area in external view (Fig. 59), head pole of the RVVC in advalvar view (Fig. 61), entire RVVC in advalvar view (Fig. 60). Scale bars: 3 µm (Figs 55–56, 60), 2 µm (Fig. 57), 1 µm (Figs 58–59, 61).
FIGURES 49–54 in New Amphicocconeis (Bacillariophyta) from Raivavae and Tahiti Islands (South Pacific) and Porto Belo (Brazil), with re-examination of Psammococconeis
FIGURES 49–54. Amphicocconeis ruatara sp. nov. SEM (material RAI 20 from Raivavae, Austral Islands, South Pacific). SV in external view, note the axial rows of long areolae, crista marginalis and marginal row of small and dense areolae (Figs 49–50), SV in internal view (Fig. 51), SVVC in advalvar view with short fused fimbriae (Fig. 52), detail of the SVVC head pole with low fimbriae (Fig. 53), and irregular rows of pores (Fig. 54). Scale bars: 3 µm (Figs 49–52), 1 µm (Figs 53–54).
FIGURES 69–72 in New Amphicocconeis (Bacillariophyta) from Raivavae and Tahiti Islands (South Pacific) and Porto Belo (Brazil), with re-examination of Psammococconeis
FIGURES 69–72. SEM (material from Raivavae, Tahiti and Moorea Isls, South Pacific). SVVC in abvalvar view of Amphicocconeis cf. mascarenica (Figs 69–70), SVVC of Amphicocconeis ruatara sp. nov. (Fig. 71), RVVC of Amphicocconeis sp. (Fig. 72). Scale bars: 1 µm (Fig. 71), 6 µm (Fig. 1), 0.5 µm (Figs 69–70), 600 nm (Fig. 72).
FIGURES 45–48 in New Amphicocconeis (Bacillariophyta) from Raivavae and Tahiti Islands (South Pacific) and Porto Belo (Brazil), with re-examination of Psammococconeis
FIGURES 45–48. Amphicocconeis antiqua sp. nov. SEM (material 'Papeete 4 Holothuria', from Tahiti, South Pacific). RV in internal view with RVVC still in place (abvalvar view) with dense rows of simple pores close to the edge of the copula (Fig. 45), foot pole of the RVVC (abvalvar view) with parallel endings around the raphe and helictoglossa (Fig. 46, twin arrowheads), detached RVVC in advalvar view (Fig. 47), RVVC in abvalvar view with radiate rows of simple pores and narrow edge void of pores (Fig. 48, arrow). Scale bars: 5 µm (Fig. 45), 4 µm (Fig. 47), 2 µm (Figs 46, 48).
FIGURES 35–40 in New Amphicocconeis (Bacillariophyta) from Raivavae and Tahiti Islands (South Pacific) and Porto Belo (Brazil), with re-examination of Psammococconeis
FIGURES 35–40. Amphicocconeis antiqua sp. nov. SEM (material 'Papeete 4 Holothuria', from Tahiti, South Pacific). SVs in external view, note the elliptic sternum with cupules (Figs 35, 37, twin arrows), ogival apices and almost no shorter striae (Figs 35–36), SV areolae in external view, with straight and narrow opening and cupules (Figs 37–38), SVVC with simple fimbriae (Fig. 40, arrowhead), SV in internal view, with elliptic large sternum and narrow hymenes (Fig. 38). Scale bars: 6 µm (Fig. 36), 5 µm (Fig. 35), 4 µm (Fig. 39), 3 µm (Figs 38, 40), 1 µm (Fig. 37).
FIGURES 30–34 in New Amphicocconeis (Bacillariophyta) from Raivavae and Tahiti Islands (South Pacific) and Porto Belo (Brazil), with re-examination of Psammococconeis
FIGURES 30–34. Amphicocconeis clypeus sp. nov. SEM (material 'Papeete 4 Holothuria', from Tahiti, South Pacific). RVVC in abvalvar view, with rows or irregular pores, with a large edge devoid of pores (Fig. 30, arrowhead), note the plow-sock (Figs 30, 33, arrows) at the head pole of the RVVC and marginal convex border (Figs 30–31), RVVC in advalvar view, with complex pores (Figs 32–33). Scale bars: 4 µm (Fig. 33), 3 µm (Fig. 30), 1 µm (Figs 31, 34), 600 nm (Fig. 32).
FIGURES 24–29 in New Amphicocconeis (Bacillariophyta) from Raivavae and Tahiti Islands (South Pacific) and Porto Belo (Brazil), with re-examination of Psammococconeis
FIGURES 24–29. Amphicocconeis clypeus sp. nov. SEM (material 'Papeete 4 Holothuria', from Tahiti, South Pacific). RV in external view with interrupted macro-areolae delineating a large lunar-shaped area void of ornamentation (Fig. 24), note the eroded macro-areolae giving access to the abvalvar side of the RVVC with complex marginal pores (Fig. 29), RV in internal view with the RVVC still in place (Fig. 25), RV in internal view (Fig. 27), detail of the central area in internal view (Fig. 26), detail of the internal apex with unraised/low helictoglossa (Fig. 28). Scale bars: 5 µm (Figs 24, 27), 4 µm (Fig. 25), 2 µm (Figs 26, 28), 400 nm (Fig. 29).
FIGURES 13–17 in New Amphicocconeis (Bacillariophyta) from Raivavae and Tahiti Islands (South Pacific) and Porto Belo (Brazil), with re-examination of Psammococconeis
FIGURES 13–17. Amphicocconeis catharinensis sp. nov. SEM (Brazilian material ICN n° 91485, Zimbros, Porto Belo, Brazil). RV in external view with marginal macro-areolae, short macro-areolae on each side of the raphe, and spread shorter areolae in between (Fig. 13), curved distal raphe endings (Fig. 15, arrowhead), proximal raphe endings curved in same side (Fig. 16), entire frustule showing the RV in internal view (Fig. 14), RVVC with oblong marginal pores in same number as the RV striae (Fig. 17, twin arrowheads). Scale bars: 4 µm (Figs 13, 17), 3 µm (Fig. 14), 1 µm (Figs 15, 16).
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
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