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Supplementary material 2 from: Gutiérrez-Gutiérrez C, Teixeira Santos M, Inácio ML, Eisenback JD, Mota M (2020) Description of Longidorus bordonensis sp. nov. from Portugal, with systematics and molecular phylogeny of the genus (Nematoda, Longidoridae). Zoosystematics and Evolution 96(1): 175-193. https://doi.org/10.3897/zse.96.49022
Figure S2
Supplementary material 4 from: Gutiérrez-Gutiérrez C, Teixeira Santos M, Inácio ML, Eisenback JD, Mota M (2020) Description of Longidorus bordonensis sp. nov. from Portugal, with systematics and molecular phylogeny of the genus (Nematoda, Longidoridae). Zoosystematics and Evolution 96(1): 175-193. https://doi.org/10.3897/zse.96.49022
Table S2
Supplementary material 1 from: Gutiérrez-Gutiérrez C, Teixeira Santos M, Inácio ML, Eisenback JD, Mota M (2020) Description of Longidorus bordonensis sp. nov. from Portugal, with systematics and molecular phylogeny of the genus (Nematoda, Longidoridae). Zoosystematics and Evolution 96(1): 175-193. https://doi.org/10.3897/zse.96.49022
Figure S1
Figure 5 from: Gutiérrez-Gutiérrez C, Teixeira Santos M, Inácio ML, Eisenback JD, Mota M (2020) Description of Longidorus bordonensis sp. nov. from Portugal, with systematics and molecular phylogeny of the genus (Nematoda, Longidoridae). Zoosystematics and Evolution 96(1): 175-193. https://doi.org/10.3897/zse.96.49022
Figure 5 Phylogenetic relationships of Longidorus bordonensis sp. nov., L. wicuolea Archidona-Yuste, Navas-Cortés, Cantalapiedra-Navarrete, Palomares-Rius & Castillo, L. vinearum Bravo & Roca and L. vineacola Sturhan & Weischer, 1964 within the genus Longidorus. Bayesian 50% majority rule consensus trees as inferred from ITS1 rRNA sequences alignments under the SYM model. Posterior probabilities more than 70% are given for appropriate clades. Newly obtained sequences in this study are coloured in green. Scale bar: expected changes per site.
Figure 4 from: Gutiérrez-Gutiérrez C, Teixeira Santos M, Inácio ML, Eisenback JD, Mota M (2020) Description of Longidorus bordonensis sp. nov. from Portugal, with systematics and molecular phylogeny of the genus (Nematoda, Longidoridae). Zoosystematics and Evolution 96(1): 175-193. https://doi.org/10.3897/zse.96.49022
Figure 4 Phylogenetic relationships of Longidorus bordonensis sp. nov. and L. vineacola Sturhan & Weischer, 1964 within the genera Longidorus and Paralongidorus. Bayesian 50% majority rule consensus trees as inferred from 18S rRNA sequences alignments under the SYM model. Posterior probabilities more than 70% are given for appropriate clades. Newly obtained sequences in this study are coloured in light blue. Scale bar: expected changes per site.
Supplementary material 5 from: Gutiérrez-Gutiérrez C, Teixeira Santos M, Inácio ML, Eisenback JD, Mota M (2020) Description of Longidorus bordonensis sp. nov. from Portugal, with systematics and molecular phylogeny of the genus (Nematoda, Longidoridae). Zoosystematics and Evolution 96(1): 175-193. https://doi.org/10.3897/zse.96.49022
Table S3
Figure 3 from: Gutiérrez-Gutiérrez C, Teixeira Santos M, Inácio ML, Eisenback JD, Mota M (2020) Description of Longidorus bordonensis sp. nov. from Portugal, with systematics and molecular phylogeny of the genus (Nematoda, Longidoridae). Zoosystematics and Evolution 96(1): 175-193. https://doi.org/10.3897/zse.96.49022
Figure 3 Phylogenetic relationships of Longidorus bordonensis sp. nov., L. wicuolea Archidona-Yuste, Navas-Cortés, Cantalapiedra-Navarrete, Palomares-Rius & Castillo, L. lusitanicus Macara, 1986, L. vinearum Bravo & Roca and L. vineacola Sturhan & Weischer, 1964 within the genus Longidorus. Bayesian 50% majority rule consensus trees as inferred from D2–D3 expansion segments of 28S rRNA sequences alignments under the SYM model. Posterior probabilities more than 70% are given for appropriate clades. Newly obtained sequences in this study are coloured in purple. Scale bar: expected changes per site.
Figure 1 from: Gutiérrez-Gutiérrez C, Teixeira Santos M, Inácio ML, Eisenback JD, Mota M (2020) Description of Longidorus bordonensis sp. nov. from Portugal, with systematics and molecular phylogeny of the genus (Nematoda, Longidoridae). Zoosystematics and Evolution 96(1): 175-193. https://doi.org/10.3897/zse.96.49022
Figure 1 Line drawings of Longidorus bordonensis sp. nov. paratypes from the rhizosphere of grass (unknown species) at São Pedro do Sul, Viseu district, northern Portugal (1–7). 1. Female anterior end. 2. Female lip region. 3. Female tail region. 4. Spicule and lateral guiding piece of gubernaculum. 5. Vulva region. 6. Male tail region. 7. Detail of basal pharyngeal bulb. Scale bars: 23 μm (1–3); 24 μm (4, 6); 29 μm (5); 15 μm (7).
Supplementary material 6 from: Gutiérrez-Gutiérrez C, Teixeira Santos M, Inácio ML, Eisenback JD, Mota M (2020) Description of Longidorus bordonensis sp. nov. from Portugal, with systematics and molecular phylogeny of the genus (Nematoda, Longidoridae). Zoosystematics and Evolution 96(1): 175-193. https://doi.org/10.3897/zse.96.49022
Table S4
Figure 2 from: Gutiérrez-Gutiérrez C, Teixeira Santos M, Inácio ML, Eisenback JD, Mota M (2020) Description of Longidorus bordonensis sp. nov. from Portugal, with systematics and molecular phylogeny of the genus (Nematoda, Longidoridae). Zoosystematics and Evolution 96(1): 175-193. https://doi.org/10.3897/zse.96.49022
Figure 2 Light micrographs of Longidorus bordonensis sp. nov. paratypes from the rhizosphere of grass (unknown species) at São Pedro do Sul, Viseu district, northern Portugal (1–10). 1. Anterior region. 2. Odontostyle region. 3. Lip region showing amphidial fovea. 4. Odontophore region. 5. Detail of basal bulb. 6, 7. Female tail region. 8. Male tail region. 9. vulva region. 10. Detail of spicule region. Abbreviations: a anus, af amphidial fovea, cd cardia, gr guiding ring, ost odontostyle, odph odontophore, sp spicules, spl ventromedian supplements, V vulva, vg vagina. Scale bars: 23 μm (1, 4); 15 μm (2, 3, 5); 50 μm (6, 7); 25 μm (8, 10); 30 μm (9).
Fig. 5 in Xibalbanus cozumelensis, a new species of Remipedia (Crustacea) from Cozumel, Mexico, and a molecular phylogeny of Xibalbanus on the Yucatán Peninsula
Fig. 5. Xibalbanus cozumelensis sp. nov., paratype (ZMUC-CRU-4792). Cephalon and cephalic structures. Scanning electron microscopy. A. Cephalon with cephalic shield and appendages. B. Antenna 1, right side, proximal parts of dorsal and ventral branches. C–D. Unidentified suctorians attached at the proximo-ventral parts of antenna 1. E. Labrum, frontal filaments, and parts of antennae 1 and 2, right side. F. Frontal filaments. G. Antenna 2, left side from anterior. H. Mandible, left side from anterior. I. Mandible, left side from posterior. J. Mandible, left side, apical view on gnathal edge. K. Mandible, left side, apical view on molar process.
Fig. 3 in Xibalbanus cozumelensis, a new species of Remipedia (Crustacea) from Cozumel, Mexico, and a molecular phylogeny of Xibalbanus on the Yucatán Peninsula
Fig. 3. Xibalbanus cozumelensis sp. nov., light microscopy. A. Holotype, adult specimen, lateral view (ZMUC-CRU-4791). B. Holotype, cephalon, lateral view. C. Paratype, cephalon, dorsal view (ZMUC- CRU-4793).
Fig. 10 in Xibalbanus cozumelensis, a new species of Remipedia (Crustacea) from Cozumel, Mexico, and a molecular phylogeny of Xibalbanus on the Yucatán Peninsula
Fig. 10. Xibalbanus cozumelensis sp. nov., paratype (ZMUC-CRU-4792), cephalon, body segments, and trunk limbs, scanning electron microscopy. A. Cephalon, cephalic shield, and head appendages from lateral. B. Trunk segments 5–10. C. Trunk limb 2, right side. D. Close-up of serrated setae in latero-distal corner of exopod segment 1. E. Close-up of serrated setae in latero-distal corner of exopod segment 2. F–G. Two unidentified suctorians attached to exopod of trunk limb 3. H–I. Posterior body segments, trunk limbs, and caudal rami from ventral and lateral.
Supplementary material 2 from: Wang P, Che J, Liu Q, Li K, Jin JQ, Jiang K, Shi L, Guo P (2020) A revised taxonomy of Asian snail-eating snakes Pareas (Squamata, Pareidae): evidence from morphological comparison and molecular phylogeny. ZooKeys 939: 45-64. https://doi.org/10.3897/zookeys.939.49309
Appendix S2
Supplementary material 1 from: Wang P, Che J, Liu Q, Li K, Jin JQ, Jiang K, Shi L, Guo P (2020) A revised taxonomy of Asian snail-eating snakes Pareas (Squamata, Pareidae): evidence from morphological comparison and molecular phylogeny. ZooKeys 939: 45-64. https://doi.org/10.3897/zookeys.939.49309
Appendix S1
Supplementary material 4 from: Wang P, Che J, Liu Q, Li K, Jin JQ, Jiang K, Shi L, Guo P (2020) A revised taxonomy of Asian snail-eating snakes Pareas (Squamata, Pareidae): evidence from morphological comparison and molecular phylogeny. ZooKeys 939: 45-64. https://doi.org/10.3897/zookeys.939.49309
Figure 1
Figure 3 from: Wang P, Che J, Liu Q, Li K, Jin JQ, Jiang K, Shi L, Guo P (2020) A revised taxonomy of Asian snail-eating snakes Pareas (Squamata, Pareidae): evidence from morphological comparison and molecular phylogeny. ZooKeys 939: 45-64. https://doi.org/10.3897/zookeys.939.49309
Figure 3 The comparisons of dorsal head (row 1) and median dorsal (row 2) between Pareas macularius and P. margaritophorus. AP. margaritophorusBP. macularius.
Figure 2 from: Wang P, Che J, Liu Q, Li K, Jin JQ, Jiang K, Shi L, Guo P (2020) A revised taxonomy of Asian snail-eating snakes Pareas (Squamata, Pareidae): evidence from morphological comparison and molecular phylogeny. ZooKeys 939: 45-64. https://doi.org/10.3897/zookeys.939.49309
Figure 2 Bayesian inference(left) and Maximum Likelihood(right) trees of the Pareidae based on mtDNA dataset. Branch support measures are Bayesian posterior probabilities and ML bootstrap support respectively. Branch support indices are not given for most intrageneric nodes to preserve clarity.
Supplementary material 3 from: Wang P, Che J, Liu Q, Li K, Jin JQ, Jiang K, Shi L, Guo P (2020) A revised taxonomy of Asian snail-eating snakes Pareas (Squamata, Pareidae): evidence from morphological comparison and molecular phylogeny. ZooKeys 939: 45-64. https://doi.org/10.3897/zookeys.939.49309
Appendix S3
Figure 1 from: Wang P, Che J, Liu Q, Li K, Jin JQ, Jiang K, Shi L, Guo P (2020) A revised taxonomy of Asian snail-eating snakes Pareas (Squamata, Pareidae): evidence from morphological comparison and molecular phylogeny. ZooKeys 939: 45-64. https://doi.org/10.3897/zookeys.939.49309
Figure 1 Bayesian inference tree of the Pareidae based on nDNA dataset. Branch support measures are Bayesian posterior probabilities/ML bootstrap support (only where >50%). Branch support indices are not given for most intrageneric nodes to preserve clarity.
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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.
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.