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Figures 38-43 from: Vitecek S, Martini J, Zittra C, Kuhlmann H, Vieira A, Waringer J (2020) The larva of Drusus dudor Oláh, 2017, including an updated key to larval Drusinae Banks, 1916 (Insecta, Trichoptera, Limnephilidae). ZooKeys 908: 137-155. https://doi.org/10.3897/zookeys.908.47032
Figures 38-43 38–39. Abdominal sterna I of 5th instar larvae, ventral views. 38Drusus camerinus Moretti, 1981 (dotted ovals: fused setal bases) 39Drusus aprutiensis Moretti, 1981. 40–41. Heads and pronota of 5th instar larvae, right lateral views. 40Drusus aprutiensis Moretti, 1981 (dotted line: base of flat pronotal hump) 41Drusus croaticus Marinkovic-Gospodnetic, 1971 (dotted line: base of high pronotal hump). 42–43. Meso- and metanota of 5th instar larvae, dorsal views. 42Drusus croaticus Marinkovic-Gospodnetic, 1971 (w: width, l: length of anterior metanotal sclerite) 43Drusus mixtus (Pictet, 1834) (w: width, l: length of anterior metanotal sclerite). Scale bars: 0.5 mm.
Figures 44-49 from: Vitecek S, Martini J, Zittra C, Kuhlmann H, Vieira A, Waringer J (2020) The larva of Drusus dudor Oláh, 2017, including an updated key to larval Drusinae Banks, 1916 (Insecta, Trichoptera, Limnephilidae). ZooKeys 908: 137-155. https://doi.org/10.3897/zookeys.908.47032
Figures 44-49 44–46. Heads and pronota of 5th instar larvae, right lateral views. 44Drusus mixtus (Pictet, 1834) (dotted line: base of high pronotal hump) 45Drusus bolivari (McLachlan, 1880) 46Drusus chauvinianus (Stein, 1874) (= Anomalopterygella chauviniana (Stein, 1874). 47–48. Heads and pronota of 5th instar larvae, frontal views. 47Drusus bolivari (McLachlan, 1880) 48Drusus chauvinianus (Stein, 1874) (= Anomalopterygella chauviniana (Stein, 1874). 49Drusus ramae Marinkovic-Gospodnetic, 1971, 5th instar larva, pronotum, right lateral view. Scale bars: 0.5 mm.
Figures 30-37 from: Vitecek S, Martini J, Zittra C, Kuhlmann H, Vieira A, Waringer J (2020) The larva of Drusus dudor Oláh, 2017, including an updated key to larval Drusinae Banks, 1916 (Insecta, Trichoptera, Limnephilidae). ZooKeys 908: 137-155. https://doi.org/10.3897/zookeys.908.47032
Figures 30-37 30–33 Abdominal sterna I of 5th instar larvae, ventral views. 30Drusus nigrescens Meyer-Duer, 1875 31Drusus franzressli Malicky, 1974 32Drusus aprutiensis Moretti, 1981 33Drusus mixtus (Pictet, 1834). 34–35 Right hind tibiae of 5th instar larvae, anterior views. 34Drusus melanchaetes McLachlan, 1876 (des: dorsal edge setae) 35Drusus monticola McLachlan, 1876 (des: dorsal edge setae). 36–37 Pronota of 5th instar larvae, right lateral views. 36Drusus vinconi Sipahiler, 1992 37Drusus ingridae Sipahiler, 1993. Scale bars: 0.5 mm.
Figures 50-57 from: Vitecek S, Martini J, Zittra C, Kuhlmann H, Vieira A, Waringer J (2020) The larva of Drusus dudor Oláh, 2017, including an updated key to larval Drusinae Banks, 1916 (Insecta, Trichoptera, Limnephilidae). ZooKeys 908: 137-155. https://doi.org/10.3897/zookeys.908.47032
Figures 50-57 50.Drusus monticola McLachlan, 1876, 5th instar larva, pronotum, right lateral view. 51–52. Heads and pronota of 5th instar larvae, frontal views. 51Drusus ramae Marinkovic-Gospodnetic, 1971 (arrow: deep V-shaped pronotal notch) 52Drusus monticola McLachlan, 1876 (arrow: shallow V-shaped pronotal notch). 53–54. Heads and pronota of 5th instar larvae, right lateral views. 53Ecclisopteryx asterix Malicky, 1979 54Drusus zivici Kučinić, Previšić, Stojanović & Vitecek, 2017. 55Ecclisopteryx asterix Malicky, 1979, 5th instar larva, head and pronotum, frontal view. 56–57. Metanota of 5th instar larvae, dorsal views. 56Ecclisopteryx asterix Malicky, 1979 (w: width, l: length of anterior metanotal sclerite) 57Drusus zivici Kučinić, Previšić, Stojanović & Vitecek, 2017 (w: width, l: length of anterior metanotal sclerite). Scale bars: 0.5 mm.
Supplementary material 1 from: Duarte S, Vieira PE, Costa FO (2020) Assessment of species gaps in DNA barcode libraries of non-indigenous species (NIS) occurring in European coastal regions. Metabarcoding and Metagenomics 4: e55162. https://doi.org/10.3897/mbmg.4.55162
Supplementary figures and tables used to analyse the data
Supplementary material 1 from: Zamora-Marín JM, Ruiz-Navarro A, Oficialdegui FJ, Anastácio PM, Miranda R, García-Murillo P, Cobo F, Ribeiro F, Gallardo B, García-Berthou E, Boix D, Medina L, Morcillo F, Oscoz J, Guillén A, Herrero-Reyes AA, Aguiar FC, Almeida D, Arias A, Ayres C, Banha F, Barca S, Biurrun I, Cabezas MP, Calero S, Campos JA, Capdevila-Argüelles L, Capinha C, Carapeto A, Casals F, Chainho P, Cirujano S, Clavero M, Cuesta JA, Deltoro V, Encarnação J, Fernández-Delgado C, Franco J, García-Meseguer AJ, Guareschi S, Guerrero-Gómez A, Hermoso V, López-Cañizares C, López-Soriano J, Machordom A, Martelo J, Mellado-Díaz A, Moreno JC, Olivo del Amo R, Otero JC, Perdices A, Pou-Rovira Q, Quiñonero-Salgado S, Rodríguez-Merino A, Ros M, Sánchez-Gullón E, Sánchez MI, Sánchez-Fernández D, Sánchez-González JR, Soriano O, Teodósio MA, Torralva M, Vieira-Lanero R, Zamora-López A, Oliva-Paterna FJ (2023) A multi-taxa assessment of aquatic non-indigenous species introduced into Iberian freshwater and transitional waters. NeoBiota 89: 17-44. https://doi.org/10.3897/neobiota.89.105994
All data of the recorded NIS
Supplementary material 2 from: Zamora-Marín JM, Ruiz-Navarro A, Oficialdegui FJ, Anastácio PM, Miranda R, García-Murillo P, Cobo F, Ribeiro F, Gallardo B, García-Berthou E, Boix D, Medina L, Morcillo F, Oscoz J, Guillén A, Herrero-Reyes AA, Aguiar FC, Almeida D, Arias A, Ayres C, Banha F, Barca S, Biurrun I, Cabezas MP, Calero S, Campos JA, Capdevila-Argüelles L, Capinha C, Carapeto A, Casals F, Chainho P, Cirujano S, Clavero M, Cuesta JA, Deltoro V, Encarnação J, Fernández-Delgado C, Franco J, García-Meseguer AJ, Guareschi S, Guerrero-Gómez A, Hermoso V, López-Cañizares C, López-Soriano J, Machordom A, Martelo J, Mellado-Díaz A, Moreno JC, Olivo del Amo R, Otero JC, Perdices A, Pou-Rovira Q, Quiñonero-Salgado S, Rodríguez-Merino A, Ros M, Sánchez-Gullón E, Sánchez MI, Sánchez-Fernández D, Sánchez-González JR, Soriano O, Teodósio MA, Torralva M, Vieira-Lanero R, Zamora-López A, Oliva-Paterna FJ (2023) A multi-taxa assessment of aquatic non-indigenous species introduced into Iberian freshwater and transitional waters. NeoBiota 89: 17-44. https://doi.org/10.3897/neobiota.89.105994
Supplementary images
Supplementary material 3 from: Arteaga A, Pyron RA, Batista A, Vieira J, Meneses Pelayo E, Smith EN, Barrio Amorós CL, Koch C, Agne S, Valencia JH, Bustamante L, Harris KJ (2024) Systematic revision of the Eyelash Palm-Pitviper Bothriechis schlegelii (Serpentes, Viperidae), with the description of five new species and revalidation of three. Evolutionary Systematics 8(1): 15-64. https://doi.org/10.3897/evolsyst.8.114527
Locality data used to create distribution maps
Supplementary material 2 from: Arteaga A, Pyron RA, Batista A, Vieira J, Meneses Pelayo E, Smith EN, Barrio Amorós CL, Koch C, Agne S, Valencia JH, Bustamante L, Harris KJ (2024) Systematic revision of the Eyelash Palm-Pitviper Bothriechis schlegelii (Serpentes, Viperidae), with the description of five new species and revalidation of three. Evolutionary Systematics 8(1): 15-64. https://doi.org/10.3897/evolsyst.8.114527
GenBank accession numbers
Supplementary material 1 from: Radulovici AE, Vieira PE, Duarte S, Teixeira MAL, Borges LMS, Deagle BE, Majaneva S, Redmond N, Schultz JA, Costa FO (2021) Revision and annotation of DNA barcode records for marine invertebrates: report of the 8 th iBOL conference hackathon. Metabarcoding and Metagenomics 5: e67862. https://doi.org/10.3897/mbmg.5.67862
Figure S1 and Tables S1–S10
Supplementary material 1 from: Leite BR, Vieira PE, Troncoso JS, Costa FO (2021) Comparing species detection success between molecular markers in DNA metabarcoding of coastal macroinvertebrates. Metabarcoding and Metagenomics 5: e70063. https://doi.org/10.3897/mbmg.5.70063
Table S1, Figures S1–S5
Supplementary material 2 from: Leite BR, Vieira PE, Troncoso JS, Costa FO (2021) Comparing species detection success between molecular markers in DNA metabarcoding of coastal macroinvertebrates. Metabarcoding and Metagenomics 5: e70063. https://doi.org/10.3897/mbmg.5.70063
Tables S2, S3
Supplementary material 2 from: Arteaga A, Quezada A, Vieira J, Guayasamin JM (2022) Leaving no stone unturned: three additional new species of Atractus ground snakes (Serpentes, Colubridae) from Ecuador discovered using a biogeographical approach. ZooKeys 1121: 175-210. https://doi.org/10.3897/zookeys.1121.89539
Figure S1
Supplementary material 1 from: Arteaga A, Quezada A, Vieira J, Guayasamin JM (2022) Leaving no stone unturned: three additional new species of Atractus ground snakes (Serpentes, Colubridae) from Ecuador discovered using a biogeographical approach. ZooKeys 1121: 175-210. https://doi.org/10.3897/zookeys.1121.89539
Table S1
Figure 4 from: Arteaga A, Mebert K, Valencia JH, Cisneros-Heredia DF, Peñafiel N, Reyes-Puig C, Vieira-Fernandes JL, Guayasamin JM (2017) Molecular phylogeny of Atractus (Serpentes, Dipsadidae), with emphasis on Ecuadorian species and the description of three new taxa. ZooKeys 661: 91-123. https://doi.org/10.3897/zookeys.661.11224
Figure 4 - Distribution of Ecuadorian snakes of the Atractus roulei species group. Dots represent known localities.
Figure 1 from: Arteaga A, Mebert K, Valencia JH, Cisneros-Heredia DF, Peñafiel N, Reyes-Puig C, Vieira-Fernandes JL, Guayasamin JM (2017) Molecular phylogeny of Atractus (Serpentes, Dipsadidae), with emphasis on Ecuadorian species and the description of three new taxa. ZooKeys 661: 91-123. https://doi.org/10.3897/zookeys.661.11224
Figure 1 - Bayesian consensus phylogeny depicting relationships within colubrid snakes of the genus Atractus, summarized from 5 million post-burnin generations in MrBayes 3.2.0. The topology was derived from analysis of 2,564 bp of mitochondrial DNA (gene fragments 16S, Cytb and ND4). Numbers next to branches correspond to posterior probability values. PP values on intraspecific branches are not shown for clarity. Voucher numbers for sequences are indicated for each terminal when available.
Figure 3 from: Arteaga A, Mebert K, Valencia JH, Cisneros-Heredia DF, Peñafiel N, Reyes-Puig C, Vieira-Fernandes JL, Guayasamin JM (2017) Molecular phylogeny of Atractus (Serpentes, Dipsadidae), with emphasis on Ecuadorian species and the description of three new taxa. ZooKeys 661: 91-123. https://doi.org/10.3897/zookeys.661.11224
Figure 3 - Distribution of Ecuadorian snakes of the Atractus iridescens species group. Dots represent known localities.
Figure 2 from: Arteaga A, Mebert K, Valencia JH, Cisneros-Heredia DF, Peñafiel N, Reyes-Puig C, Vieira-Fernandes JL, Guayasamin JM (2017) Molecular phylogeny of Atractus (Serpentes, Dipsadidae), with emphasis on Ecuadorian species and the description of three new taxa. ZooKeys 661: 91-123. https://doi.org/10.3897/zookeys.661.11224
Figure 2 - Photographs of some Ecuadorian species of Atractus in life: Atractus carrioni MZUTI 4194 (a), MZUTI 4195 (b), Atractus duboisi MZUTI 3640 (c), Atractus dunni MZUTI 4318 (d), Atractus dunni MZUTI 2189 (e), Atractus elaps AMARU SN (f), Atractus gigas MZUTI 3286 (g), Atractus iridescens MZUTI 3680 (h), Atractus iridescens QCAZ 8072 (i), Atractus iridescens MZUTI 4697 (j), Atractus iridescens MZUTI 3548 (k), Atractus major MZUTI 4973 (l), Atractus microrhynchus MZUTI 5109 (m), Atractus modestus (n), Atractus multicinctus MZUTI 5106 (o), Atractus occidentalis MZUTI 1385 (p), Atractus occidentalis MZUTI 3323 (q), Atractus paucidens MZUTI 5102 (r), Atractus resplendens MZUTI 3996 (s), Atractus roulei MZUTI 4503 (t), Atractus savagei MZUTI 4916 (u), Atractus snethlageae (v), Atractus touzeti ANF 2390 (w), and Atractus typhon MZUTI 5110.
Figure 6 from: Arteaga A, Mebert K, Valencia JH, Cisneros-Heredia DF, Peñafiel N, Reyes-Puig C, Vieira-Fernandes JL, Guayasamin JM (2017) Molecular phylogeny of Atractus (Serpentes, Dipsadidae), with emphasis on Ecuadorian species and the description of three new taxa. ZooKeys 661: 91-123. https://doi.org/10.3897/zookeys.661.11224
Figure 6 - Adult male holotype of Atractus esepe MZUTI 3758 in dorsal (a) and ventral (b) view. Scale = 1 cm.
Figure 5 from: Arteaga A, Mebert K, Valencia JH, Cisneros-Heredia DF, Peñafiel N, Reyes-Puig C, Vieira-Fernandes JL, Guayasamin JM (2017) Molecular phylogeny of Atractus (Serpentes, Dipsadidae), with emphasis on Ecuadorian species and the description of three new taxa. ZooKeys 661: 91-123. https://doi.org/10.3897/zookeys.661.11224
Figure 5 - Adult male holotype MZUTI 4330 (a) and adult male paratopotype (b) of Atractus cerberus MZUTI 5108.
ScienceDex guides
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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)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
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.
International Brain Laboratory public data
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
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.