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zenodo28/100

Figure 9-17 from: Pinedo-Escatel JA, Dmitriev D (2019) Redescription of the Dikraneurini leafhopper Dikrella mella Ruppel & DeLong, 1952 (Hemiptera, Cicadellidae) with a synoptic checklist of leafhoppers on avocado trees in Mexico. ZooKeys 857: 17-27. https://doi.org/10.3897/zookeys.857.33910

Figure 9-17 Morphological structures of microleafhopper (Typhlocybinae) species associated to avocado trees in Mexico 9 forewing of Idonadmitrievi10 hind wing of Idonadmitrievi11 forewing of Idonafloresi12 hind wing of Jorumakrausi13 aedeagus of Alconeuracandida14 pygofer of Empoascaangustella, lateral view 15 pygofer of Idonadmitrievi, lateral view 16 pygofer of Idonagonzalezae, lateral view 17 pygofer of Idonaminuenda, lateral view.

opencc-by-4.0Jul 2019View details →
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Figure 5 from: Compton JA, Schrire BD, Könyves K, Forest F, Malakasi P, Mattapha S, Sirichamorn Y (2019) The Callerya Group redefined and Tribe Wisterieae (Fabaceae) emended based on morphology and data from nuclear and chloroplast DNA sequences. PhytoKeys 125: 1-112. https://doi.org/10.3897/phytokeys.125.34877

Figure 5 Wisteriopsisjaponica (Siebold & Zucc.) J.Compton & Schrire. A Habit B stipels C lower surface of leaflet D flower bud with bract and bracteoles E flower F1 calyx outer surface F2 calyx inner surface and detail of hairs G standard petal inner surface H wing petal I keel petal J staminal column K ovary and style L pods M pod interior and seed N ventral view of seed O lateral view of seed A–C, E–K from Maximowicz s.n.. 1863 D from Oldham 386, L–O from Togasi MSM1, 1950. Drawn by Margaret Tebbs.

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

Plate 1 from: Compton JA, Schrire BD, Könyves K, Forest F, Malakasi P, Mattapha S, Sirichamorn Y (2019) The Callerya Group redefined and Tribe Wisterieae (Fabaceae) emended based on morphology and data from nuclear and chloroplast DNA sequences. PhytoKeys 125: 1-112. https://doi.org/10.3897/phytokeys.125.34877

Plate 1 Endosamara, Sigmoidala and Kanburia. A, BEndosamararacemosa, Thailand, Sakon Nakhon Prov., S.Mattapha s.n.. C, DSigmoidalakityana Thailand, Nan Prov. S.Mattapha 1117EKanburiachlorantha Thailand, Kanchanaburi Prov. Y.Sirichamorn Y2014-15-1FKanburiatenasserimensis Thailand, Ratchaburi, Khao Chon waterfall Y.Sirichamorn YS2015-8.

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

Plate 3 from: Compton JA, Schrire BD, Könyves K, Forest F, Malakasi P, Mattapha S, Sirichamorn Y (2019) The Callerya Group redefined and Tribe Wisterieae (Fabaceae) emended based on morphology and data from nuclear and chloroplast DNA sequences. PhytoKeys 125: 1-112. https://doi.org/10.3897/phytokeys.125.34877

Plate 3 Wisteriopsis and Wisteria. AWisteriopsisjaponica, Cultivated, J.C.Raulston Arboretum, North Carolina 980008-17 BWisteriopsisjaponica Japan, Honshu near Kyoto G.Lewis, unvouchered C, DWisteriopsisjaponica, Cultivated, J.C.Raulston Arboretum, North Carolina 980008-17 EWisteriopsisreticulata Cultivated, J.Compton s.n.. unvouchered FWisteriafrutescens Cultivated, B.Schrire unvouchered GWisteriabrachybotrys cultivated, B.Schrire unvouchered.

opencc-by-4.0Jul 2019View details →
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Figure 4 from: Compton JA, Schrire BD, Könyves K, Forest F, Malakasi P, Mattapha S, Sirichamorn Y (2019) The Callerya Group redefined and Tribe Wisterieae (Fabaceae) emended based on morphology and data from nuclear and chloroplast DNA sequences. PhytoKeys 125: 1-112. https://doi.org/10.3897/phytokeys.125.34877

Figure 4 Nanhaiaspeciosa (Champ. ex Benth.) J.Compton & Schrire. A Habit B flower bud with bract and bracteole C calyx exterior and bracteole D detail of calyx exterior E detail of calyx interior F standard petal G wing petal H keel petal I staminal column J staminal column lateral view K stamen ventral and dorsal view L ovary and style M style and stigma N pod O seed lateral view P seed ventral view (all from Shiu Ling Hu 6091). Drawn by Margaret Tebbs.

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

Figure 2 from: Compton JA, Schrire BD, Könyves K, Forest F, Malakasi P, Mattapha S, Sirichamorn Y (2019) The Callerya Group redefined and Tribe Wisterieae (Fabaceae) emended based on morphology and data from nuclear and chloroplast DNA sequences. PhytoKeys 125: 1-112. https://doi.org/10.3897/phytokeys.125.34877

Figure 2 Distinctive morphological characters in Tribe Wisterieae. AEndosamararacemosa standard petal inner surface BPadbruggeadasyphylla standard petal inner surface CPadbruggeadasyphylla pod DPadbruggeadasyphylla seed lateral view EAustrocalleryaaustralis standard petal inner surface FAustrocalleryapilipes pod GAustrocalleryapilipes seed lateral view HPadbruggeafilipes standard petal IAfgekiasericea standard petal inner surface JAfgekiasericea seed lateral view KAfgekiasericea seed angled lateral view LCalleryanitida pod MCalleryanitida seed ventral view NCalleryanitida seed polar view OCalleryacinerea pod PWhitfordiodendronnieuwenhuisii pod QWhitfordiodendronerianthum seed RWisteriopsiseurybotrya gibbosity SWisteriopsischampionii gibbosity A from Luang Vanpruk 188 B from Scortechini 429 C, D from Lamb 395/91 E from L.J.Brass 32129 F, G from B.Gray 04319 H from Maung Po Khant 15326 I from C. Chermsirivathana 996 J, K from Mrs Collins 104/9 L–N from Theophilus SampsonO from G.Forrest 19279 P from J.P.Mogea 4182 Q from photo Y.Sirichamorn s.n..R from J. & M.S.Clemens 3637 S from Shiu Ying Hu 10476. See Appendix 1 for voucher details. Drawn by Margaret Tebbs.

opencc-by-4.0Jul 2019View details →
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Supplementary material 1 from: Compton JA, Schrire BD, Könyves K, Forest F, Malakasi P, Mattapha S, Sirichamorn Y (2019) The Callerya Group redefined and Tribe Wisterieae (Fabaceae) emended based on morphology and data from nuclear and chloroplast DNA sequences. PhytoKeys 125: 1-112. https://doi.org/10.3897/phytokeys.125.34877

: Data type: molecular data

opencc-zeroJul 2019View details →
zenodo28/100

Figure 1 from: Compton JA, Schrire BD, Könyves K, Forest F, Malakasi P, Mattapha S, Sirichamorn Y (2019) The Callerya Group redefined and Tribe Wisterieae (Fabaceae) emended based on morphology and data from nuclear and chloroplast DNA sequences. PhytoKeys 125: 1-112. https://doi.org/10.3897/phytokeys.125.34877

Figure 1 Combined Maximum Liklihood (ML) and Bayesian Inference (BI) Phylogenetic tree of Tribe Wisterieae. The tree is derived from the combined plastid and ITS, RAxML bipartitions analysis representing 77 (36) ingroup samples (taxa) and 59 (40) outgroup samples (taxa). The outgroup Schefflerodendron is used to root the trees. Lines in bold on the phylogeny incorporate results from the combined Bayesian Inference analysis, demarcating clades with BPP (0.95) support and above. Nodes are marked up with bootstrap values as percentages derived from the combined ML analysis with values of 50% or less marked in red. The collapsed portion of the tree, below the IRLC and above Schefflerodendron, represents the following genera (see Suppl. material 1: Figs S1–S6): Tribe Robinieae (Coursetia, Gliricidia, Poissonia & Poitea); Tribe Sesbanieae (Sesbania), Tribe Loteae (Coronilla, Lotus & Securigera); Tribe Millettieae (Millettia), Tribe Abreae (Abrus); Tribe Phaseoleae (Clitoria & Ophrestia); Tribe Indigofereae (Phylloxylon) and basal millettioids (Austrosteenisia, Disynstemon, Xeroderris & Platycyamus). Tribe Wisterieae is treated within five clades (Clades A–E), colour coded green for Clade A (Sarcodum, Endosamara & Sigmoidala); cyan for Clade B (Nanhaia & Wisteriopsis), red for Clade C (Callerya, Serawaia, Whitfordiodendron, Kanburia & Afgekia); orange for Clade D (Padbruggea & Austrocallerya) and yellow for Clade E (Wisteria). Each clade is further subdivided to represent the genera (except for the single accession of Serawaia which is incorporated with Whitfordiodendron in Clade C2) and E1 and E2 represent the geographical disjunction of species in Wisteria. Outgroups within the IRLC in purple include Glycyrrhiza, Adinobotrys and representatives of the Temperate Tribe block. The ingroup (IRLC) and Tribe Wisterieae are demarcated with arrows on the tree.

opencc-by-4.0Jul 2019View details →
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Figure 6 from: Compton JA, Schrire BD, Könyves K, Forest F, Malakasi P, Mattapha S, Sirichamorn Y (2019) The Callerya Group redefined and Tribe Wisterieae (Fabaceae) emended based on morphology and data from nuclear and chloroplast DNA sequences. PhytoKeys 125: 1-112. https://doi.org/10.3897/phytokeys.125.34877

Figure 6 Austrocalleryaaustralis (Endl.) J.Compton & Schrire. A Habit B leaf and detail of leaflet apex C flower buds with bract and 2 bracteoles D flower E calyx external surface F calyx detail of inner surface G standard petal inner surface H wing petal I keel petal J staminal column ventral view K stamens dorsal and ventral views L staminal column lateral view M ovary lateral view N stigma O pod P seed angled lateral view (all from Martin 1392). Drawn by Margaret Tebbs.

opencc-by-4.0Jul 2019View details →
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Figure 3 from: Compton JA, Schrire BD, Könyves K, Forest F, Malakasi P, Mattapha S, Sirichamorn Y (2019) The Callerya Group redefined and Tribe Wisterieae (Fabaceae) emended based on morphology and data from nuclear and chloroplast DNA sequences. PhytoKeys 125: 1-112. https://doi.org/10.3897/phytokeys.125.34877

Figure 3 Sigmoidalakityana (Craib) J.Compton & Schrire. A Habit B young leaf C lower surface of leaf D leaflet detail of hairs E inflorescence F flower bud with bracteole and pedicel G calyx external surface H standard petal inner surface I wing petal J keel petal K staminal column lateral view L staminal column ventral view M stamen dorsal and ventral views N ovary lateral view O style and stigma P pod Q pod detail of surface R seed ventral view S seed lateral view (all from Clark 245). Drawn by Margaret Tebbs.

opencc-by-4.0Jul 2019View details →
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Plate 2 from: Compton JA, Schrire BD, Könyves K, Forest F, Malakasi P, Mattapha S, Sirichamorn Y (2019) The Callerya Group redefined and Tribe Wisterieae (Fabaceae) emended based on morphology and data from nuclear and chloroplast DNA sequences. PhytoKeys 125: 1-112. https://doi.org/10.3897/phytokeys.125.34877

Plate 2 Afgekia, Sarcodum and Padbruggea. AAfgekiamahidoliae, Thailand, Sai Yok distr. Kanchanaburi, Y.Sirichamorn s.n.. B, CAfgekiasericea Thailand S.Mattapha 1158DSarcodumscandens Vietnam, Quang Binh Prov. Lôc & Quang P11554EAfgekiamahidiliae Thailand, Sai Yok distr. Kanchanaburi Y.Sirichamorn s.n.. FSarcodumscandens Vietnam, Quang Binh Prov. Lôc & Quang P11554GSarcodumscandens Laos, Sop Teuang, Bolikhamxai Prov. S.Lanorsavanh 1299H, IPadbruggeafilipes Thailand, Chiang Mai, Y.Sirichamorn & S.Mattapha YSM2017-1.

opencc-by-4.0Jul 2019View details →
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Supplementary material 1 from: Yackel Adams AA, Nafus MG, Klug PE, Lardner B, Mazurek MJ, Savidge JA, Reed RN (2019) Contact rates with nesting birds before and after invasive snake removal: estimating the effects of trap-based control. NeoBiota 49: 1-17. https://doi.org/10.3897/neobiota.49.35592

: Data type: TIF File (.tif)

opencc-zeroJul 2019View details →
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Supplementary material 2 from: Feng C, Miller JA, Lin Y, Shu Y (2019) Further study of two Chinese cave spiders (Araneae, Mysmenidae), with description of a new genus. ZooKeys 870: 77-100. https://doi.org/10.3897/zookeys.870.35971

Uncorrected pairwise distances based on full alignment

opencc-zeroAug 2019View details →
zenodo28/100

Supplementary material 1 from: Feng C, Miller JA, Lin Y, Shu Y (2019) Further study of two Chinese cave spiders (Araneae, Mysmenidae), with description of a new genus. ZooKeys 870: 77-100. https://doi.org/10.3897/zookeys.870.35971

Alignment of DNA sequence data used in phylogenetic analyses

opencc-zeroAug 2019View details →
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Figure 1 from: Orsenigo S, Astuti G, Bartolucci F, Citterio S, Conti F, Garrido-Becerra JA, Gentili R, del Galdo GG, Jiménez-Martínez JF, Karrer G, Lahora A, Martínez-Hernández F, Mendoza-Fernández AJ, Merlo ME, Montagnani C, Mota J, Nicolella G, Pérez-García FJ, Peruzzi L, Robles J, Roma-Marzio F, Salmerón-Sánchez E, Sánchez-Gómez P, Serra L, Stinca A, Fenu G (2017) Global and Regional IUCN Red List Assessments: 3. Italian Botanist 3: 83-98. https://doi.org/10.3897/italianbotanist.3.13303

Figure 1 - Individual in bud of Crepis lacera subsp. titani on limestone cliffs of Monte Titano (San Marino Republic). Photograph by L. Peruzzi.

opencc-by-4.0Jun 2017View details →
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Figure 8 from: Orsenigo S, Astuti G, Bartolucci F, Citterio S, Conti F, Garrido-Becerra JA, Gentili R, del Galdo GG, Jiménez-Martínez JF, Karrer G, Lahora A, Martínez-Hernández F, Mendoza-Fernández AJ, Merlo ME, Montagnani C, Mota J, Nicolella G, Pérez-García FJ, Peruzzi L, Robles J, Roma-Marzio F, Salmerón-Sánchez E, Sánchez-Gómez P, Serra L, Stinca A, Fenu G (2017) Global and Regional IUCN Red List Assessments: 3. Italian Botanist 3: 83-98. https://doi.org/10.3897/italianbotanist.3.13303

Figure 8 - Italian distribution map of Ambrosia maritima based only on verified sites and herbarium specimens.

opencc-by-4.0Jun 2017View details →
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Figure 5 from: Orsenigo S, Astuti G, Bartolucci F, Citterio S, Conti F, Garrido-Becerra JA, Gentili R, del Galdo GG, Jiménez-Martínez JF, Karrer G, Lahora A, Martínez-Hernández F, Mendoza-Fernández AJ, Merlo ME, Montagnani C, Mota J, Nicolella G, Pérez-García FJ, Peruzzi L, Robles J, Roma-Marzio F, Salmerón-Sánchez E, Sánchez-Gómez P, Serra L, Stinca A, Fenu G (2017) Global and Regional IUCN Red List Assessments: 3. Italian Botanist 3: 83-98. https://doi.org/10.3897/italianbotanist.3.13303

Figure 5 - Flowers of Commicarpus plumbagineus in Sierra de Orihuela (Alicante, Spain). Photograph by L. Serra.

opencc-by-4.0Jun 2017View details →
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Figure 7 from: Orsenigo S, Astuti G, Bartolucci F, Citterio S, Conti F, Garrido-Becerra JA, Gentili R, del Galdo GG, Jiménez-Martínez JF, Karrer G, Lahora A, Martínez-Hernández F, Mendoza-Fernández AJ, Merlo ME, Montagnani C, Mota J, Nicolella G, Pérez-García FJ, Peruzzi L, Robles J, Roma-Marzio F, Salmerón-Sánchez E, Sánchez-Gómez P, Serra L, Stinca A, Fenu G (2017) Global and Regional IUCN Red List Assessments: 3. Italian Botanist 3: 83-98. https://doi.org/10.3897/italianbotanist.3.13303

Figure 7 - Ambrosia maritima in Sardinia: plants in their coastal dunes habitat, comparison between leaves of A. maritima and exotic ragweeds A. artemisiifolia (a) and A. psilostachya (b). Photographs by C. Montagnani.

opencc-by-4.0Jun 2017View details →
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Figure 6 from: Orsenigo S, Astuti G, Bartolucci F, Citterio S, Conti F, Garrido-Becerra JA, Gentili R, del Galdo GG, Jiménez-Martínez JF, Karrer G, Lahora A, Martínez-Hernández F, Mendoza-Fernández AJ, Merlo ME, Montagnani C, Mota J, Nicolella G, Pérez-García FJ, Peruzzi L, Robles J, Roma-Marzio F, Salmerón-Sánchez E, Sánchez-Gómez P, Serra L, Stinca A, Fenu G (2017) Global and Regional IUCN Red List Assessments: 3. Italian Botanist 3: 83-98. https://doi.org/10.3897/italianbotanist.3.13303

Figure 6 - Extent of occurrence (orange) and area of occupancy (red) of Commicarpus plumbagineus in Spain.

opencc-by-4.0Jun 2017View details →
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Figure 9 from: Feng C, Miller JA, Lin Y, Shu Y (2019) Further study of two Chinese cave spiders (Araneae, Mysmenidae), with description of a new genus. ZooKeys 870: 77-100. https://doi.org/10.3897/zookeys.870.35971

Figure 9 Yamaneta paquini (Miller, Griswold & Yin, 2009) comb. nov. from Lushui Co., Daxingdi, Walayaku [cave], female genitalia A, B Epigyne C–D vulva (lactic acid treated) A, C ventral B lateral D dorsal. Unlabeled arrow in B indicates curved profile of dorsal surface of scape, in D indicates notched lateral margin of scape. Abbreviations: CD copulatory ducts; FD fertilization ducts; S spermathecae; Sp scape. Scale bars: 0.10 mm.

opencc-by-4.0Oct 2019View details →

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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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