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Figure 2 from: Sukhorukov AP, Nilova MV, Krinitsina AA, Zaika MA, Erst AS, Shepherd KA (2018) Molecular phylogenetic data and seed coat anatomy resolve the generic position of some critical Chenopodioideae (Chenopodiaceae – Amaranthaceae) with reduced perianth segments. PhytoKeys 109: 103-128. https://doi.org/10.3897/phytokeys.109.28956

Figure 2 Best tree from the BEAST analysis of the combined trnL-trnF + rbcL + atpB-rbcLChenopodioideae dataset. Bayesian posterior probabilities are given above the branches, jackknife values (left) and bootstrap percentages of the maximum likelihood analyses (right) are given below branches.

opencc-by-4.0Oct 2018View details →
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Figure 8 from: Sukhorukov AP, Nilova MV, Krinitsina AA, Zaika MA, Erst AS, Shepherd KA (2018) Molecular phylogenetic data and seed coat anatomy resolve the generic position of some critical Chenopodioideae (Chenopodiaceae – Amaranthaceae) with reduced perianth segments. PhytoKeys 109: 103-128. https://doi.org/10.3897/phytokeys.109.28956

Figure 8 SEM detail of the inflorescence of Neomonolepisspathulata. Abbreviations: B – bract (stained in green), FF – female flowers (orange), MF –male flower (perianth stained in blue, stamen in yellow), S – stem.

opencc-by-4.0Oct 2018View details →
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Figure 7 from: Niu W, Yu S, Tian P, Xiao J (2018) Complete mitochondrial genome of Echinophyllia aspera (Scleractinia, Lobophylliidae): Mitogenome characterization and phylogenetic positioning. ZooKeys 793: 1-14. https://doi.org/10.3897/zookeys.793.28977

Figure 7 Inferred phylogenetic relationships based on the concatenated nucleotide sequences of 13 mitochondrial protein-coding genes using Bayesian inference (BI) and maximum likelihood (ML). Numbers on branches are Bayesian posterior probabilities and bootstrap percentages.

opencc-by-4.0Nov 2018View details →
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Figure 2 from: Niu W, Yu S, Tian P, Xiao J (2018) Complete mitochondrial genome of Echinophyllia aspera (Scleractinia, Lobophylliidae): Mitogenome characterization and phylogenetic positioning. ZooKeys 793: 1-14. https://doi.org/10.3897/zookeys.793.28977

Figure 2 The mitochondrial genome of Echinophylliaaspera. Gene order and positions are shown; all the genes are encoded on H-strand. COI, COII, COIII refer to the cytochrome oxidase subunits, Cyt b refers to cytochrome b, ND1-ND6 refer to NADH dehydrogenase components.

opencc-by-4.0Nov 2018View details →
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Supplementary material 1 from: Forero D, Rodríguez J, Ocampo V (2018) A new species of Carvalhomiris from Colombia with an assessment of its phylogenetic position (Heteroptera, Miridae, Orthotylinae). In: Wheeler Jr AG (Ed.) A Festschrift Recognizing Thomas J. Henry for a Lifetime of Contributions to Heteropteran Systematics. ZooKeys 796: 197-214. https://doi.org/10.3897/zookeys.796.22058

Carvalhomiris matrix (phylogenetic) :

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Figure 6 from: Forero D, Rodríguez J, Ocampo V (2018) A new species of Carvalhomiris from Colombia with an assessment of its phylogenetic position (Heteroptera, Miridae, Orthotylinae). In: Wheeler Jr AG (Ed.) A Festschrift Recognizing Thomas J. Henry for a Lifetime of Contributions to Heteropteran Systematics. ZooKeys 796: 197-214. https://doi.org/10.3897/zookeys.796.22058

Figure 6 Phylogenetic analysis of Carvalhomiris species, including C.henryi sp. n. A One of the two trees obtained (Ci: 81, Ri: 67) with characters and character states indicated on the branches B consensus tree of the two trees obtained.

opencc-by-4.0Nov 2018View details →
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Figure 2 from: Forero D, Rodríguez J, Ocampo V (2018) A new species of Carvalhomiris from Colombia with an assessment of its phylogenetic position (Heteroptera, Miridae, Orthotylinae). In: Wheeler Jr AG (Ed.) A Festschrift Recognizing Thomas J. Henry for a Lifetime of Contributions to Heteropteran Systematics. ZooKeys 796: 197-214. https://doi.org/10.3897/zookeys.796.22058

Figure 2 Carvalhomirishenryi sp. n. Male genitalia. A Right paramere, lateral right view B–D left paramere B caudal view C dorsal view D medial view. Arrows on C and D show the dorsal process E, F genital capsule E caudal view F lateral left view G, H aedeagus, not everted G lateral right view H dorsal view.

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Figure 5 from: Forero D, Rodríguez J, Ocampo V (2018) A new species of Carvalhomiris from Colombia with an assessment of its phylogenetic position (Heteroptera, Miridae, Orthotylinae). In: Wheeler Jr AG (Ed.) A Festschrift Recognizing Thomas J. Henry for a Lifetime of Contributions to Heteropteran Systematics. ZooKeys 796: 197-214. https://doi.org/10.3897/zookeys.796.22058

Figure 5 Distribution map of species of Carvalhomiris, including C.henryi sp. n. (modified from Forero 2009).

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Figure 4 from: Forero D, Rodríguez J, Ocampo V (2018) A new species of Carvalhomiris from Colombia with an assessment of its phylogenetic position (Heteroptera, Miridae, Orthotylinae). In: Wheeler Jr AG (Ed.) A Festschrift Recognizing Thomas J. Henry for a Lifetime of Contributions to Heteropteran Systematics. ZooKeys 796: 197-214. https://doi.org/10.3897/zookeys.796.22058

Figure 4 A Roadside vegetation in a montane cloud forest on the road to Ventanas, where C.henryi sp. n. was found BAcmella sp. (Asteraceae), plant on which specimens of C.henryi sp. n. were found.

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Figure 3 from: Forero D, Rodríguez J, Ocampo V (2018) A new species of Carvalhomiris from Colombia with an assessment of its phylogenetic position (Heteroptera, Miridae, Orthotylinae). In: Wheeler Jr AG (Ed.) A Festschrift Recognizing Thomas J. Henry for a Lifetime of Contributions to Heteropteran Systematics. ZooKeys 796: 197-214. https://doi.org/10.3897/zookeys.796.22058

Figure 3 Carvalhomirishenryi sp. n. Female genitalia. A Dorsal labiate plate and sclerotized rings, dorsal view B anterior wall, anterior view, showing the vestibulum, indicating the asymmetrical medial margin of gonapophysis 8 C posterior wall, dorsal view, showing the interramal dorsal processes.

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Figure 1 from: Forero D, Rodríguez J, Ocampo V (2018) A new species of Carvalhomiris from Colombia with an assessment of its phylogenetic position (Heteroptera, Miridae, Orthotylinae). In: Wheeler Jr AG (Ed.) A Festschrift Recognizing Thomas J. Henry for a Lifetime of Contributions to Heteropteran Systematics. ZooKeys 796: 197-214. https://doi.org/10.3897/zookeys.796.22058

Figure 1 Carvalhomirishenryi sp. n. Dorsal habitus images. Male and female brachypterous specimens (upper row), and male and female macropterous specimens (bottom row). The male brachypterous specimen is the holotype.

opencc-by-4.0Nov 2018View details →
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Supplementary material 1 from: Wu R-W, Liu X-J, Wang S, Roe KJ, Ouyang S, Wu X-P (2019) Analysis of mitochondrial genomes resolves the phylogenetic position of Chinese freshwater mussels (Bivalvia, Unionidae). ZooKeys 812: 23-46. https://doi.org/10.3897/zookeys.812.29908

: Data type: molecular data

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Figure 4 from: Wu R-W, Liu X-J, Wang S, Roe KJ, Ouyang S, Wu X-P (2019) Analysis of mitochondrial genomes resolves the phylogenetic position of Chinese freshwater mussels (Bivalvia, Unionidae). ZooKeys 812: 23-46. https://doi.org/10.3897/zookeys.812.29908

Figure 4 Hypotheses of phylogenetic relationships among subfamilies of the Unionidae form this and other studies. ALopes-Lima et al. (2017a)BBolotov et al. (2017a)CHuang et al. 2013; Burzyński et al. 2017; Huang et al. 2018; Wu et al. 2016, 2017bD This study.

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Figure 2 from: Wu R-W, Liu X-J, Wang S, Roe KJ, Ouyang S, Wu X-P (2019) Analysis of mitochondrial genomes resolves the phylogenetic position of Chinese freshwater mussels (Bivalvia, Unionidae). ZooKeys 812: 23-46. https://doi.org/10.3897/zookeys.812.29908

Figure 2 The gene arrangement of the F-type mitochondrial genome of Acuticostachinensis, Schistodesmuslampreyanus, Cuneopsisheudei, and Cuneopsiscapitatus.

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Figure 3 from: Wu R-W, Liu X-J, Wang S, Roe KJ, Ouyang S, Wu X-P (2019) Analysis of mitochondrial genomes resolves the phylogenetic position of Chinese freshwater mussels (Bivalvia, Unionidae). ZooKeys 812: 23-46. https://doi.org/10.3897/zookeys.812.29908

Figure 3 Phylogenetic trees of freshwater mussels obtained by Bayesian Inference (BI) and Maximum Likelihood (ML) analyses of 12 mitochondrial protein-coding gene sequences (except atp8) and two rRNA combined dataset. Support values above the branches are posterior probabilities and bootstrap support. (*) indicates 100 percent bootstrap support and posterior probabilities. Red font indicates Chinese species.

opencc-by-4.0Jan 2019View details →
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Figure 1 from: Wu R-W, Liu X-J, Wang S, Roe KJ, Ouyang S, Wu X-P (2019) Analysis of mitochondrial genomes resolves the phylogenetic position of Chinese freshwater mussels (Bivalvia, Unionidae). ZooKeys 812: 23-46. https://doi.org/10.3897/zookeys.812.29908

Figure 1 Shells of the unionids species in this study. AAcuticostachinensis (Lea, 1868) BSchistodesmuslampreyanus (Baird & Adams, 1867) CCuneopsisheudei (Heude, 1874) DCuneopsiscapitatus (Heude, 1874). Scale bar: 4 cm. Photogaphs R-W Wu.

opencc-by-4.0Jan 2019View details →
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Figure 7 from: Ng PKL, Priyaja P, Kumar AB, Devi SS (2019) A collection of crabs (Crustacea, Brachyura) from the southwestern coast of India, with a discussion of the systematic position of Nectopanope Wood-Mason in Wood-Mason & Alcock, 1891 (Euryplacidae). ZooKeys 818: 1-24. https://doi.org/10.3897/zookeys.818.32108

Figure 7 Gonopods. A–ENectopanoperhodobaphes Wood-Mason in Wood-Mason & Alcock, 1891, male (18.4 × 14.7 mm) F–HHenicoplaxmaldivensis (Rathbun, 1902), male (9.9 × 6.3 mm) I–MCryptopodiacollifer Flipse, 1930, male (17.5 × 10.6 mm) N–PParaxanthodescumatodes (MacGilchrist, 1905), male (8.3 × 5.5 mm). A, F left G1 (ventral view) B, G left G1 (dorsal view) C distal part of left G1 (ventral view) D distal part of left G1 (dorsal view); left G2. Scales bars: 0.5 mm (A, B, E–H–P); 0.25 mm (C, D).

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Figure 6 from: Ng PKL, Priyaja P, Kumar AB, Devi SS (2019) A collection of crabs (Crustacea, Brachyura) from the southwestern coast of India, with a discussion of the systematic position of Nectopanope Wood-Mason in Wood-Mason & Alcock, 1891 (Euryplacidae). ZooKeys 818: 1-24. https://doi.org/10.3897/zookeys.818.32108

Figure 6 APseudolambrusbeaumonti (Alcock, 1895), female (9.4 × 8.8 mm) BRhinolambruscontrarius (Herbst, 1804), female (10.5 × 10.0 mm) C–FCryptopodiacollifer Flipse, 1930, male (17.5 × 10.6 mm) G, HParaxanthodescumatodes (MacGilchrist, 1905), male (8.3 × 5.5 mm). A, B, C, G, H overall dorsal habitus D ventral view of cephalothorax E, F outer view of chelae.

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Figure 5 from: Ng PKL, Priyaja P, Kumar AB, Devi SS (2019) A collection of crabs (Crustacea, Brachyura) from the southwestern coast of India, with a discussion of the systematic position of Nectopanope Wood-Mason in Wood-Mason & Alcock, 1891 (Euryplacidae). ZooKeys 818: 1-24. https://doi.org/10.3897/zookeys.818.32108

Figure 5 Henicoplaxmaldivensis (Rathbun, 1902), male (9.9 × 6.3 mm), India. A overall dorsal habitus B dorsal view of carapace C frontal view of cephalothorax D left third maxilliped E anterior thoracic sternum and pleon F thoracic sternum and pleon G posterior thoracic sternum and pleon H outer view of chelae.

opencc-by-4.0Jan 2019View details →
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Figure 4 from: Ng PKL, Priyaja P, Kumar AB, Devi SS (2019) A collection of crabs (Crustacea, Brachyura) from the southwestern coast of India, with a discussion of the systematic position of Nectopanope Wood-Mason in Wood-Mason & Alcock, 1891 (Euryplacidae). ZooKeys 818: 1-24. https://doi.org/10.3897/zookeys.818.32108

Figure 4 Nectopanoperhodobaphes Wood-Mason in Wood-Mason & Alcock, 1891, male (18.4 × 14.7 mm), India. A anterior thoracic sternum, pleon, buccal cavity and third maxillipeds B thoracic sternum and pleon C posterior thoracic sternum and pleon D anterior thoracic sternum and sternopleonal cavity E subdorsal view of right cheliped F inner view of right cheliped G–J second to fourth ambulatory legs, respectively (all to same scale).

opencc-by-4.0Jan 2019View details →

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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

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