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zenodo32/100

Supplementary material 4 from: Seltmann K, Lafia S, Paul D, James S, Bloom D, Rios N, Ellis S, Farrell U, Utrup J, Yost M, Davis E, Emery R, Motz G, Kimmig J, Shirey V, Sandall E, Park D, Tyrrell C, Thackurdeen R, Collins M, O'Leary V, Prestridge H, Evelyn C, Nyberg B (2018) Georeferencing for Research Use (GRU): An integrated geospatial training paradigm for biocollections researchers and data providers. Research Ideas and Outcomes 4: e32449. https://doi.org/10.3897/rio.4.e32449

Three months after the workshop, participants were surveyed to assess what workshop-related knowledge and materials were being used and disseminated to others. This document summarized data collected in this particular survey.

opencc-zeroDec 2018View details →
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Supplementary material 1 from: Seltmann K, Lafia S, Paul D, James S, Bloom D, Rios N, Ellis S, Farrell U, Utrup J, Yost M, Davis E, Emery R, Motz G, Kimmig J, Shirey V, Sandall E, Park D, Tyrrell C, Thackurdeen R, Collins M, O'Leary V, Prestridge H, Evelyn C, Nyberg B (2018) Georeferencing for Research Use (GRU): An integrated geospatial training paradigm for biocollections researchers and data providers. Research Ideas and Outcomes 4: e32449. https://doi.org/10.3897/rio.4.e32449

Darwin Core Archive file downloaded from the iDigBio portal for use in the Georeferencing for Research Use workshop. Total 25,429 records, accessed on 2016-08-29. Collections contributing to the record set are listed in the archive records.citation.txt file. Dataset GUID: a69d1541-4726-465d-84ad-50c7ed556eee

opencc-zeroDec 2018View details →
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text-fig. 5. Skull reconstructions of representatives of Jurassic OTUs in left lateral view, a, Dilophosaurus wetherilli, Early Jurassic (Sinemurian-Pliensbachian), Kayenta Formation, Arizona, USA; based on UCMP V 4214 and V 6468. B, Syntarsus rhodesiensis, Early Jurassic (Hettangian-Sinemurian), Forest Sandstone, Zimbabwe; composite reconstruction based on many isolated skull elements from the National Museum of Natural History in Harare (see Appendix), c, Magnosaurus oxoniensis, Middle Jurassic (Callovian), Oxford Clay, England; based on OUM J 13558, unpreserved elements shaded. D, Monolophosaurus jiangi, Middle Jurassic, Wucaiwan Formation, China; redrawn from Zhao and Currie (1993b). E, Allosaurus fragilis, Late Jurassic (Kimmeridgian-Tithonian), Morrison Formation, USA; based on MOR 693. f, basal bird Archaeopteryx sp., Late Jurassic (Tithonian), lithographic limestones of Solnhofen, Germany; based on Wellnhofer (1974), Elzanowski and Wellnhofer (1996), and the Berlin, Eichstätt, and Munich specimens. G, Ceratosaurus sp., Late Jurassic (Kimmeridgian-Tithonian), Morrison Formation, USA; based on USNM 4735 and UMNH VP 5278. H, Ornitholestes hermanni, Late Jurassic (Kimmeridgian-Tithonian), Morrison Formation, USA, based on AMNH 619. Abbreviations as in Text-figure 4, and: If, lacrimal fenestra; mf, maxillary fenestra; nf, nasal foramen; pmf, promaxillary fenestra. Scale bars represent 10 mm (b, f, h), 50 mm (c) and 100 mm (a, d, e, g). in The interrelationships and evolution of basal theropod dinosaurs

text-fig. 5. Skull reconstructions of representatives of Jurassic OTUs in left lateral view, a, Dilophosaurus wetherilli, Early Jurassic (Sinemurian-Pliensbachian), Kayenta Formation, Arizona, USA; based on UCMP V 4214 and V 6468. B, Syntarsus rhodesiensis, Early Jurassic (Hettangian-Sinemurian), Forest Sandstone, Zimbabwe; composite reconstruction based on many isolated skull elements from the National Museum of Natural History in Harare (see Appendix), c, Magnosaurus oxoniensis, Middle Jurassic (Callovian), Oxford Clay, England; based on OUM J 13558, unpreserved elements shaded. D, Monolophosaurus jiangi, Middle Jurassic, Wucaiwan Formation, China; redrawn from Zhao and Currie (1993b). E, Allosaurus fragilis, Late Jurassic (Kimmeridgian-Tithonian), Morrison Formation, USA; based on MOR 693. f, basal bird Archaeopteryx sp., Late Jurassic (Tithonian), lithographic limestones of Solnhofen, Germany; based on Wellnhofer (1974), Elzanowski and Wellnhofer (1996), and the Berlin, Eichstätt, and Munich specimens. G, Ceratosaurus sp., Late Jurassic (Kimmeridgian-Tithonian), Morrison Formation, USA; based on USNM 4735 and UMNH VP 5278. H, Ornitholestes hermanni, Late Jurassic (Kimmeridgian-Tithonian), Morrison Formation, USA, based on AMNH 619. Abbreviations as in Text-figure 4, and: If, lacrimal fenestra; mf, maxillary fenestra; nf, nasal foramen; pmf, promaxillary fenestra. Scale bars represent 10 mm (b, f, h), 50 mm (c) and 100 mm (a, d, e, g).

opennotspecifiedMay 2003View details →
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FIGURE 1. Lacvietina nabanhensis, male. A. Habitus. B. Tergite VIII. C. Sternite V and VI. D. Sternite VII. E. Sternite VIII. F–G in A contribution to the knowledge of the genus Lacvietina Herman (Coleoptera Staphylinidae: Tachyporinae) from China

FIGURE 1. Lacvietina nabanhensis, male. A. Habitus. B. Tergite VIII. C. Sternite V and VI. D. Sternite VII. E. Sternite VIII. F–G. Aedeagus, lateral (F) and ventral (G). Scale bars: 1.0 mm in A; 0.2 mm in B–G.

opennotspecifiedSep 2019View details →
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FIGURE 3. Angraecum gereauanum. A. Plant habit. B.–C. Stem showing flat and winged sides. D.–E. Flower. F. Dorsal sepal. G. Petals. H. Lateral sepals. I.–J. Lip with spur. K. Ovary and column. L.–Q. Column with and without anther cap seen from different angles. R.–T. Anther cap with and without pollinia. U. Pollinium. V in Taxonomy of Atlantic Central African orchids, 6: three new species of Angraecum sect. Afrangraecum (Orchidaceae, Angraecinae) from Gabon and São Tomé

FIGURE 3. Angraecum gereauanum. A. Plant habit. B.–C. Stem showing flat and winged sides. D.–E. Flower. F. Dorsal sepal. G. Petals. H. Lateral sepals. I.–J. Lip with spur. K. Ovary and column. L.–Q. Column with and without anther cap seen from different angles. R.–T. Anther cap with and without pollinia. U. Pollinium. V. Stipes and viscidia. (Drawing by Hans de Vries from Stévart, Leal & Nguema 2501.)

opennotspecifiedSep 2017View details →
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FIGURE 3. Pteridocalyx appunii. Calycophyll variation within the same inflorescence branch. A. Basal flower. B–D. Intermediate flowers, from base towards distal portion. E. Distal flower. A–E in Notes on calycophyllous Rubiaceae. Part V. A succinct overview of genera with calycophylls, and a revision of Pteridocalyx (Sipaneeae) with observations on distyly and calycophyll variation

FIGURE 3. Pteridocalyx appunii. Calycophyll variation within the same inflorescence branch. A. Basal flower. B–D. Intermediate flowers, from base towards distal portion. E. Distal flower. A–E: drawn from P.G. Delprete & P. Benjamin 12813 (CAY). Illustration by Piero Delprete.

opennotspecifiedJan 2019View details →
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FIGURE 2. Pteridocalyx appunii. A. Habit. B. Inflorescences, side view. C. Inflorescence, top view. D. Corolla, top view. E in Notes on calycophyllous Rubiaceae. Part V. A succinct overview of genera with calycophylls, and a revision of Pteridocalyx (Sipaneeae) with observations on distyly and calycophyll variation

FIGURE 2. Pteridocalyx appunii. A. Habit. B. Inflorescences, side view. C. Inflorescence, top view. D. Corolla, top view. E. Inflorescence and infructescence from the same plant. Photos by Piero Delprete.

opennotspecifiedJan 2019View details →
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FIGURE 4. A–E Stage V, F–H Stage VI and I– K Stage VII. A in Larval development of the shrimp Hippolyte sapphica d'Udekem d'Acoz, 1993 forma A and B (Decapoda: Caridea: Hippolytidae) reared in the laboratory, confirmation of the conspecific status of the two forms

FIGURE 4. A–E Stage V, F–H Stage VI and I– K Stage VII. A. Telson; B. Uropod; C. 3rd Maxilliped; D. 1st Pereiopod; E. 2nd Pereiopod; F. Telson; G. 1st Maxilliped; H. 2nd Maxilliped; I. 1st and 2nd Pleopods; J. Telson; K. Antennula. Scales: A. 0.015mm; B. 0.040mm; C. 0.003mm; D. 0.0011mm; E. 0.028mm; F. 0.038mm; G. 0.066mm; H. 0.028mm; I. 0.019mm; J. 0.039mm; K. 0.046mm.

opennotspecifiedAug 2010View details →
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FIGURE 1 in A REVIEW OF THE SYSTEMATICS OF THE TICK FAMILY ARGASIDAE (IXODIDA) Agustín E -P , Atilio J. M , Santiago N , JosØ M. V ,

FIGURE 1: See next page

opencc-by-nd-4.0Sep 2010View details →
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FIGURE. Typical habitats of Ramalina species on northern South America. A. High paramo, Laguna Anteojos, Sierra Nevada de Merida, where grows on rocks R. anteojina at 4100 m. B. Sub-paramo (timberline), La Aguada, Sierra Nevada de Merida, 3100 m, where are found R. dictyota and R. reducta on shrubs. C. Andean cloud forest, La Victoria, Sierra Nevada de Merida where R. cochlearis, R. cumanensis and R. victoriana are found growing as epiphytes. D. Populations of R. usnea, R. morrocoyensis and R. paradisensis growing as epiphytes on mangroves and Suriana maritima at sea level, National Park Morrocoy, state Falcón; the latter two species are known only from this locality. E. Ramalina usnea is the only species of this genus reported from the Alto Orinoco, Amazonas, near La Esmeralda, 150 m, growing as corticolous in submontane forests, at the top of the picture the Cerro Duida. F. Xerophytic forests from the National Park Cerro Santa Ana, state Falcón, where Ramalina santanensis and R. microphylla are known only growing on soil and rocks at 200–400 m. Photos V. Marcano. in The genus Ramalina Acharius (Ascomycota, Lecanoromycetes, Ramalinaceae) in northern South America

FIGURE. Typical habitats of Ramalina species on northern South America. A. High paramo, Laguna Anteojos, Sierra Nevada de Merida, where grows on rocks R. anteojina at 4100 m. B. Sub-paramo (timberline), La Aguada, Sierra Nevada de Merida, 3100 m, where are found R. dictyota and R. reducta on shrubs. C. Andean cloud forest, La Victoria, Sierra Nevada de Merida where R. cochlearis, R. cumanensis and R. victoriana are found growing as epiphytes. D. Populations of R. usnea, R. morrocoyensis and R. paradisensis growing as epiphytes on mangroves and Suriana maritima at sea level, National Park Morrocoy, state Falcón; the latter two species are known only from this locality. E. Ramalina usnea is the only species of this genus reported from the Alto Orinoco, Amazonas, near La Esmeralda, 150 m, growing as corticolous in submontane forests, at the top of the picture the Cerro Duida. F. Xerophytic forests from the National Park Cerro Santa Ana, state Falcón, where Ramalina santanensis and R. microphylla are known only growing on soil and rocks at 200–400 m. Photos V. Marcano.

opennotspecifiedMay 2021View details →
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FIGURE. Fruits of the genera and subgenera of Bromelioideae. A. Acanthostachys pitcairnioides (Leme 483). B. Acanthostachys strobilacea (Leme 8306). C. Aechmea subg. Platyaechmea s.str.: A. caesia (Leme 3588). D. Aechmea subg. Lamprococcus: A capixabae (Leme 6948). E. Aechmea of the "Streptocalycoid complex": A. nidularioides (Leme 2150). F. Wittmackia lingulatoides (Leme 9585). G–H. Aechmea of the "Gravisia complex". G. A. aquilega (Leme 9516). H. A. blanchetiana (Leme 8890). I–L. Aechmea subg. Chevaliera s.l. I. A. castanea (Leme 6940). J. A. digitata (Leme 4019). K. A. fernandae (Leme 4492). L. A. ornata (Leme 6760). M. Greigia stenolepis (Leme 9738). N. Bromelia antiacantha (Leme 258). O. Bromelia aff. reversacantha (Leme 4609). P–Q. Billbergia subg. Billbergia. P. B. amoena var. amoena (Leme 6168). Q. B. amoena var. stolonifera (Leme 215-B). R. Billbergia subg. Helicodea: B. zebrina (Leme 128). S. Cryptanthus tabuleiricola (Leme 8014). T. Billbergia (Pseudaechmea) viridiflora (SEL 99-026). U. Portea petropolitana var. noetiigii (Leme 5277). V. Hohenbergia lanata (Leme 9625). W. Quesnelia quesneliana (Leme 107). X. Fernseea bocainensis (Leme 1422). Y. Disteganthus lateralis (Leme 9390). Z. Neoglaziovia variegata (Leme 9631). a. Aechmea subg. Pothuava s.l.: A. roberto-seidelii (Leme 1203). b. Aechmea subg. Macrochordion: A. bruggeri (Leme 4765). c. Araeococcus flagellifolius (Leme 9501). Bars = 10 mm. in Re-evaluation of the Amazonian Hylaeaicum (Bromeliaceae: Bromelioideae) based on neglected morphological traits and molecular evidence

FIGURE. Fruits of the genera and subgenera of Bromelioideae. A. Acanthostachys pitcairnioides (Leme 483). B. Acanthostachys strobilacea (Leme 8306). C. Aechmea subg. Platyaechmea s.str.: A. caesia (Leme 3588). D. Aechmea subg. Lamprococcus: A capixabae (Leme 6948). E. Aechmea of the "Streptocalycoid complex": A. nidularioides (Leme 2150). F. Wittmackia lingulatoides (Leme 9585). G–H. Aechmea of the "Gravisia complex". G. A. aquilega (Leme 9516). H. A. blanchetiana (Leme 8890). I–L. Aechmea subg. Chevaliera s.l. I. A. castanea (Leme 6940). J. A. digitata (Leme 4019). K. A. fernandae (Leme 4492). L. A. ornata (Leme 6760). M. Greigia stenolepis (Leme 9738). N. Bromelia antiacantha (Leme 258). O. Bromelia aff. reversacantha (Leme 4609). P–Q. Billbergia subg. Billbergia. P. B. amoena var. amoena (Leme 6168). Q. B. amoena var. stolonifera (Leme 215-B). R. Billbergia subg. Helicodea: B. zebrina (Leme 128). S. Cryptanthus tabuleiricola (Leme 8014). T. Billbergia (Pseudaechmea) viridiflora (SEL 99-026). U. Portea petropolitana var. noetiigii (Leme 5277). V. Hohenbergia lanata (Leme 9625). W. Quesnelia quesneliana (Leme 107). X. Fernseea bocainensis (Leme 1422). Y. Disteganthus lateralis (Leme 9390). Z. Neoglaziovia variegata (Leme 9631). a. Aechmea subg. Pothuava s.l.: A. roberto-seidelii (Leme 1203). b. Aechmea subg. Macrochordion: A. bruggeri (Leme 4765). c. Araeococcus flagellifolius (Leme 9501). Bars = 10 mm.

opennotspecifiedMay 2021View details →
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FIGURE. Flowers and longitudinal/cross sections of ovaries of the genera of the "Nidularioid complex" and Aechmea alliance. A. Neoregelia leucophoea (Leme 1107). B–C. Neoregelia subg. Protoregelia: N. longisepala (Leme 3049). D–E. Canistropsis burchellii (Leme 1301). F–G. Canistropsis microps (Leme 9017). H–J. Canistrum subg. Canistrum: C. aurantiacum (Leme 5028). K–L. Canistrum subg. Cucullatanthus: C. auratum (Leme 5803). M–N. Edmundoa ambigua (Leme 1073). O–P. Eduandrea selloana (Leme 7630). Q–R. Nidularium camposportoi var. robustum (Leme 3772). S–T. Nidularium rutilans (Leme 1072). U–V. Wittrockia superba (Leme 4751). W– X. Wittrockia gigantea (Leme 1289). Y–a. Aechmea aculeatosepala (Leme 3235). b–c. Aechmea castelnavii (Leme 4168). d–e. Aechmea hoppii (Leme 2339). Bars = 5 mm. in Re-evaluation of the Amazonian Hylaeaicum (Bromeliaceae: Bromelioideae) based on neglected morphological traits and molecular evidence

FIGURE. Flowers and longitudinal/cross sections of ovaries of the genera of the "Nidularioid complex" and Aechmea alliance. A. Neoregelia leucophoea (Leme 1107). B–C. Neoregelia subg. Protoregelia: N. longisepala (Leme 3049). D–E. Canistropsis burchellii (Leme 1301). F–G. Canistropsis microps (Leme 9017). H–J. Canistrum subg. Canistrum: C. aurantiacum (Leme 5028). K–L. Canistrum subg. Cucullatanthus: C. auratum (Leme 5803). M–N. Edmundoa ambigua (Leme 1073). O–P. Eduandrea selloana (Leme 7630). Q–R. Nidularium camposportoi var. robustum (Leme 3772). S–T. Nidularium rutilans (Leme 1072). U–V. Wittrockia superba (Leme 4751). W– X. Wittrockia gigantea (Leme 1289). Y–a. Aechmea aculeatosepala (Leme 3235). b–c. Aechmea castelnavii (Leme 4168). d–e. Aechmea hoppii (Leme 2339). Bars = 5 mm.

opennotspecifiedMay 2021View details →
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FIGURE. Conduplicate-spiral (CS) and cupulate (CL) stigma types of Acanthostachys, the different subgenera of Aechmea, and Karawata. A. Acanthostachys pitcairnioides (CS, Leme 483). B. Aechmea aculeatosepala (CS, Leme 3235). C–F. Aechmea subg. Aechmea. C. A. angustifolia (CS, Leme 8632). D. A. bracteata (CL, Leme 3466). E. A. phanerophlebia (CS, Leme 1472). F. A. tocantina (CS, Leme 143). G–I. Aechmea of the "Streptocalycoid complex". G. A. hoppii (CS, Leme 2339). H. A. longifolia (CS, Leme 116). I. A. vallerandii (CS, Leme 8693). J–K. Aechmea subg. Platyaechmea s.l. J. A. cucullata (CS, Leme 3462). K. A. manzanareziana (CS, Leme 3125). L. Aechmea of the "Gravisia complex": A. aquilega (CS, Leme 9516). M–N, P. Aechmea subg. Chevaliera s.l. M. A. cariocae (CS, Leme 5196). N. A. castanea (CS, Leme 1142). O. Karawata multiflora (CS, Leme 6500). P. A. ornata (CS, Leme 6760). Q–R. Aechmea subg. Macrochordion. Q. A. alba (CS, Leme 8232); R. A. bromeliifolia (CS, Leme 7951). S–T. Aechmea subg. Platyaechmea s.str. S. A. caesia (CS, Leme 3588); T. A. fasciata var. purpurea (CS, Leme 8639). U–V. Aechmea subg. Lamprococcus. U. A. capixabae (CS, Leme 6948). V. A. fulgens (CS, Leme 6209). W. Aechmea subg. Ortgiesia: A. candida (CS, Leme 9113). X. Aechmea subg. Pothuava s.str.: A. nudicaulis (CS, Leme 1436). Bars = 1 mm. in Re-evaluation of the Amazonian Hylaeaicum (Bromeliaceae: Bromelioideae) based on neglected morphological traits and molecular evidence

FIGURE. Conduplicate-spiral (CS) and cupulate (CL) stigma types of Acanthostachys, the different subgenera of Aechmea, and Karawata. A. Acanthostachys pitcairnioides (CS, Leme 483). B. Aechmea aculeatosepala (CS, Leme 3235). C–F. Aechmea subg. Aechmea. C. A. angustifolia (CS, Leme 8632). D. A. bracteata (CL, Leme 3466). E. A. phanerophlebia (CS, Leme 1472). F. A. tocantina (CS, Leme 143). G–I. Aechmea of the "Streptocalycoid complex". G. A. hoppii (CS, Leme 2339). H. A. longifolia (CS, Leme 116). I. A. vallerandii (CS, Leme 8693). J–K. Aechmea subg. Platyaechmea s.l. J. A. cucullata (CS, Leme 3462). K. A. manzanareziana (CS, Leme 3125). L. Aechmea of the "Gravisia complex": A. aquilega (CS, Leme 9516). M–N, P. Aechmea subg. Chevaliera s.l. M. A. cariocae (CS, Leme 5196). N. A. castanea (CS, Leme 1142). O. Karawata multiflora (CS, Leme 6500). P. A. ornata (CS, Leme 6760). Q–R. Aechmea subg. Macrochordion. Q. A. alba (CS, Leme 8232); R. A. bromeliifolia (CS, Leme 7951). S–T. Aechmea subg. Platyaechmea s.str. S. A. caesia (CS, Leme 3588); T. A. fasciata var. purpurea (CS, Leme 8639). U–V. Aechmea subg. Lamprococcus. U. A. capixabae (CS, Leme 6948). V. A. fulgens (CS, Leme 6209). W. Aechmea subg. Ortgiesia: A. candida (CS, Leme 9113). X. Aechmea subg. Pothuava s.str.: A. nudicaulis (CS, Leme 1436). Bars = 1 mm.

opennotspecifiedMay 2021View details →
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FIGURE 8. Cricotopus pupa, tergites. A. C. acornis, B. C. albitarsis, C. C. annuliventris, D. C. brevicornis, E. C in Taxonomic review of the chironomid genus Cricotopus v. d. Wulp (Diptera: Chironomidae) from Australia: keys to males, females, pupae and larvae, description of ten new species and comments on Paratrichocladius Santos Abreu

FIGURE 8. Cricotopus pupa, tergites. A. C. acornis, B. C. albitarsis, C. C. annuliventris, D. C. brevicornis, E. C. conicornis (reticulations shown only on part TVIII), F. C. hillmani

opennotspecifiedDec 2015View details →
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FIGURE 4. Cricotopus female. Spermathecae. A. C. acornis, B. C. albitarsis, C. C. annuliventris, D. C. brevicornis, E. C. conicornis, F. C. hillmani, G. C. parbicinctus, H. C. tasmania, I. C in Taxonomic review of the chironomid genus Cricotopus v. d. Wulp (Diptera: Chironomidae) from Australia: keys to males, females, pupae and larvae, description of ten new species and comments on Paratrichocladius Santos Abreu

FIGURE 4. Cricotopus female. Spermathecae. A. C. acornis, B. C. albitarsis, C. C. annuliventris, D. C. brevicornis, E. C. conicornis, F. C. hillmani, G. C. parbicinctus, H. C. tasmania, I. C. varicornis.

opennotspecifiedDec 2015View details →
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FIGURE 9. Cricotopus pupa, tergites. A. C. howensis, B. C. parbicinctus, C. C. tasmania, D. C. varicornis, E. C in Taxonomic review of the chironomid genus Cricotopus v. d. Wulp (Diptera: Chironomidae) from Australia: keys to males, females, pupae and larvae, description of ten new species and comments on Paratrichocladius Santos Abreu

FIGURE 9. Cricotopus pupa, tergites. A. C. howensis, B. C. parbicinctus, C. C. tasmania, D. C. varicornis, E. C. wangi.

opennotspecifiedDec 2015View details →
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FIGURE 1. A–C. Valeriana plateadensis. D–E. V. yacuriensis. F–G. V. xenophylloides. A, D, F. Habit. B in Three new species of Valeriana (Valerianoideae, Caprifoliaceae) from southern Ecuador

FIGURE 1. A–C. Valeriana plateadensis. D–E. V. yacuriensis. F–G. V. xenophylloides. A, D, F. Habit. B. Close up of branches. C, E, G. Close up of inflorescence, showing 3-merous flowers. Photographs by Álvaro J. Pérez (A, C), Claes Persson (B), Petr Sklenář (D–G).

opennotspecifiedJan 2023View details →
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FIGURES 19a–e. Andrena transbaicalica Popov, 1949 in The type specimens of bees (Hymenoptera: Apoidea) deposited in the Zoological Institute of the Russian Academy of Sciences, St. Petersburg. Contribution VI. Family Andrenidae, genus Andrena Fabricius, 1775, taxa described by V. Popov

FIGURES 19a–e. Andrena transbaicalica Popov, 1949. Holotype, female: a—habitus, lateral view and labels; b—head, frontal view; c—labrum, dorsal view; d—T1–T3, dorsal view; e—mesosoma, dorsal view. Scale bar: 1 mm.

opennotspecifiedJun 2023View details →
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FIGURES 16a–e. Andrena skorikovi Popov, 1940 in The type specimens of bees (Hymenoptera: Apoidea) deposited in the Zoological Institute of the Russian Academy of Sciences, St. Petersburg. Contribution VI. Family Andrenidae, genus Andrena Fabricius, 1775, taxa described by V. Popov

FIGURES 16a–e. Andrena skorikovi Popov, 1940. Holotype, female: a—habitus, lateral view and labels; b—head, frontal view; c—labrum, dorsal view; d—T1–T3, dorsal view; e—mesosoma, dorsal view. Scale bar: 1 mm.

opennotspecifiedJun 2023View details →
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FIGURES 15a–e. Andrena shakuensis Popov, 1949 in The type specimens of bees (Hymenoptera: Apoidea) deposited in the Zoological Institute of the Russian Academy of Sciences, St. Petersburg. Contribution VI. Family Andrenidae, genus Andrena Fabricius, 1775, taxa described by V. Popov

FIGURES 15a–e. Andrena shakuensis Popov, 1949. Lectotype, female: a—habitus, lateral view and labels; b—head, frontal view; c—labrum, dorsal view; d—T1–T3, dorsal view; e—mesosoma, dorsal view. Scale bar: 1 mm.

opennotspecifiedJun 2023View 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

ScienceDex for faculty

Your academic CV and NIH biosketch

Make your CV in your school's format and your NIH biosketch from it, then download both as Word files.