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Figures 10–13 in Suspended mummies in Aleiodes species (Hymenoptera: Braconidae: Rogadinae) with descriptions of six new species from western Uganda based largely on DNA sequence data
Figures 10–13. Automontage photographs of features of Aleiodes busutai sp. n., habitus, head lateral aspect, metasoma and mesosoma, respectively.
Figure 2 in Suspended mummies in Aleiodes species (Hymenoptera: Braconidae: Rogadinae) with descriptions of six new species from western Uganda based largely on DNA sequence data
Figure 2. Phylogram from analysis of CO1 DNA sequence data for individuals of the A. buzurae-group and related species, and also multiple representatives of four European species for comparison.
Figure 1 in Suspended mummies in Aleiodes species (Hymenoptera: Braconidae: Rogadinae) with descriptions of six new species from western Uganda based largely on DNA sequence data
Figure 1. Photograph of a suspended mummy showing J-shaped configuration with silk thread (arrowed) arising near larval mouth.
Figure 4 in Suspended mummies in Aleiodes species (Hymenoptera: Braconidae: Rogadinae) with descriptions of six new species from western Uganda based largely on DNA sequence data
Figure 4. Selected contiguous fragment of the CO1 gene in individuals of the Aleiodes buzurae-group from Uganda and Kenya with bold characters indicating substitutions. Asterisks show phylogenetically informative substitutions at species level; exclamation marks show apomorphies for individual species in the buzarae group and $ sites that have both unique and informative variation.
Figs 1-4 in New data on Xantholinini from China. XVII. Daolus niger nov.sp. from Zhejiang (Coleoptera: Staphylinidae, Xantholinini) 205° contribution to the knowledge of the Staphylinidae
Figs 1-4: Daolus niger nov.sp: (1) labrum; (2) tergite of the male genital segment; (3) sternite of the same; (4) aedeagus (scale: 0.1 mm).
Figs 30–31. 30 in A new species and new data on distribution of the shore bugs of China (Hemiptera: Heteroptera: Saldidae)
Figs 30–31. 30 – Distribution of Macrosaldula bogdashana Luo & Vinokurov, 2011 (1) and Salda littoralis (Linnaeus, 1758) (2) in Xinjiang. 31 – distribution of Rupisalda austrosinica sp. nov.
Figs 22–29 in A new species and new data on distribution of the shore bugs of China (Hemiptera: Heteroptera: Saldidae)
Figs 22–29. Rupisalda thailandana (Cobben, 1986): 22 – forewing;, 23, 24 – paramere in various positions; 25 – parandria; 26 – penisfilum; 27 – medial endosomal sclerite; 28 – subgenital plate; 29 – spermatheca. Figures after COBBEN (1986).
Figs 32–36. 32–33 in A new species and new data on distribution of the shore bugs of China (Hemiptera: Heteroptera: Saldidae)
Figs 32–36. 32–33 – habitats of Rupisalda austrosinica sp. nov.: 32 – Danxia Shan NP, Xianglong lake, 33 – Jizu Shan Mt. 34 – habitat of Saldula burmanica Lindskog, 1975, Haba Xueshan Mts. 35–36 – habitats of Saldula recticollis (Horváth, 1899): 35 – Nanling NNR, Dadongshan; 36 – Danxia Shan NP, slopes of Elder peak (Photo: J. Hájek).
Figs 15–21 in A new species and new data on distribution of the shore bugs of China (Hemiptera: Heteroptera: Saldidae)
Figs 15–21. Rupisalda austrosinica sp. nov.: 15–17 – paramere in various positions, 18 – parandria, 19 – penisfilum, 20 – median endosomal sclerite in ventral view, 21 – spermatheca.
Figs 1–8. 1 in A new species and new data on distribution of the shore bugs of China (Hemiptera: Heteroptera: Saldidae)
Figs 1–8. 1 – Chiloxanthus kozlovi (Kiritshenko, 1912), female (Sichuan). 2–7 – Calacanthia grandis Cobben, 1985; 2 – female (Gansu); 3 – paramere; 4 – parandria; 5–6 – medial endosomal sclerite (5 – lateral view, 6 – ventral view); 7 – female, holotype, forewing (after COBBEN 1985). 8 – Macrosaldula bogdashana Luo & Vinokurov, 2011, female (Xinjiang).
Figs 9–14 in A new species and new data on distribution of the shore bugs of China (Hemiptera: Heteroptera: Saldidae)
Figs 9–14. Rupisalda austrosinica sp. nov.: 9–10 – male (Guangdong); 11 – female (Yunnan); 12 – forewing; 13 – head, frontal view; 14 – female subgenital plate, ventral view. Abbreviations: eg – eversible gland.
Fig. 31 in Andrena (Suandrena) portosanctana COCKERELL, 1922 and A. (Suandrena) maderensis COCKERELL, 1922 - new taxonomical and ecological data for two closely related endemic bee species of the Madeira Archipelago, Portugal
Fig. 31 ff.: Morphological differences between males of A. portosanctana (N = 4) and A. maderensis (N = 13): (e) labrum process width; (f) stigma length; (g) propodeum length.
Fig. 30 in Andrena (Suandrena) portosanctana COCKERELL, 1922 and A. (Suandrena) maderensis COCKERELL, 1922 - new taxonomical and ecological data for two closely related endemic bee species of the Madeira Archipelago, Portugal
Fig. 30 ff.: Morphological differences between females of A. portosanctana (N = 19) and A. maderensis (N = 30): (g) stigma length; (h) propodeum length.
Figs. 25-29 in Andrena (Suandrena) portosanctana COCKERELL, 1922 and A. (Suandrena) maderensis COCKERELL, 1922 - new taxonomical and ecological data for two closely related endemic bee species of the Madeira Archipelago, Portugal
Figs. 25-29: Male of Andrena maderensis, collected by A. Kratochwil (MA05/38: Madeira, Ponta de São Lourenço, coastal rock, partly ruderalized, 100 m, 32°44'44.01''N, -16°43'20.74''E, Leontodon taraxacoides subsp. longirostris, 26.03.2005); (25) lateral view; (26) dorsal view; (27) head frontal view; genital (28) front view, (29) sideview; photos: L. Haitzinger.
Figs. 1-4 in Andrena (Suandrena) portosanctana COCKERELL, 1922 and A. (Suandrena) maderensis COCKERELL, 1922 - new taxonomical and ecological data for two closely related endemic bee species of the Madeira Archipelago, Portugal
Figs. 1-4: Syntype of Andrena portosanctana (female) deposited in the California Academy of Science, California, San Francisco, USA (CAS TYPE 15373); (1) lateral view; (2) dorsal view; (3) head frontal view; (4) labels; photos: V. Smith.
Fig. 30 in Andrena (Suandrena) portosanctana COCKERELL, 1922 and A. (Suandrena) maderensis COCKERELL, 1922 - new taxonomical and ecological data for two closely related endemic bee species of the Madeira Archipelago, Portugal
Fig. 30: Morphological differences between females of A. portosanctana (N = 19) and A. maderensis (N = 30): (a) body length; (b) wing length; (c) head length/width index; (d) facial fovea index; (e) clypeal length; (f) labrum process width.
Figs 12-18 in New data on the Xantholinini from the Oriental Region. XXII. New species from Laos (Coleoptera, Staphylinidae) 203° contribution to the knowledge of the Staphylinidae
Figs 12-18: Oculolabrus laotianus BORDONI: tergite (12) and sternite (13) of the male genital segment, aedeagus (14); Atopolinus sulcatus BORDONI: pronotum (15), tergite (16) and sternite (17) of the male genital segment, aedeagus (18) (scale: 0.1 mm).
Figs. 9–16 in A new species of the genus Trichomyia (Diptera: Psychodidae) and new faunistic data on non-phlebotomine moth flies from the Podyjí NP and its surroundings (Czech Republic)
Figs. 9–16. Trichomyia hardeggensis sp. nov., male: 9 – head, caudal view; 10 – basal antennomeres; 11 – palpus maxillaris, dorsal view; 12 – wing; 13 – basal apodeme of aedeagal complex, dorsal view; 14 – same, lateral view; 15 – aedeagal complex and gonopods, dorsal view; 16 – gonopod and a part of aedeagus, lateral view. Scales: 11, 13–16 = 0.1 mm; 10 = 0.2 mm; 9 = 0.3 mm; 12 =1 mm.
Figs. 17–24 in A new species of the genus Trichomyia (Diptera: Psychodidae) and new faunistic data on non-phlebotomine moth flies from the Podyjí NP and its surroundings (Czech Republic)
Figs. 17–24. Trichomyia hardeggensis sp. nov., male: 17 – maxilla and maxillary palpus, lateral view; 18 – maxilla; 19 – terminal lobes of labium; 20 – thoracic sclerites, lateral view; 21 – aedeagal complex, dorsal view; 22 – same, diagonal view; 23 – epandrium and surstyli, dorsal view; 24 – same, lateral view. Scales: 18–19, 21–24 = 0.1 mm; 17, 20 = 0.2 mm.
Figs. 1–8 in A new species of the genus Trichomyia (Diptera: Psychodidae) and new faunistic data on non-phlebotomine moth flies from the Podyjí NP and its surroundings (Czech Republic)
Figs. 1–8. Trichomyia hardeggensis sp. nov., male: 1 – head (supraocular lateral bristles omitted, only setae alveoli marked); 2 – facets, caudal view of eye fold; 3 – terminal antennomeres; 4 – cibarium, epipharynx and labrum, dorsal view; 5 – thorax, fore part with spiracular area, lateral view; 6 – haltere; 7 – wing, basal part in detail; 8 – claw of P1. Scales: 2–4, 6 = 0.1 mm; 1, 5, 7 = 0.2 mm; 8 = 0.01 mm.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.