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FIGURE 5 in Taxonomic revision of Neotropical Phyllocnistis Zeller, 1848 (Lepidoptera: Gracillariidae), with descriptions of seven new species and host plant associations

FIGURE 5. Geographical distribution of Phyllocnistis species endemic to the Neotropical region.

opennotspecifiedOct 2017View details →
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FIGURE 3 in Taxonomic revision of Neotropical Phyllocnistis Zeller, 1848 (Lepidoptera: Gracillariidae), with descriptions of seven new species and host plant associations

FIGURE 3. (Continued)

opennotspecifiedOct 2017View details →
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Fig. 4 in Taxonomic Notes and New Distribution and Host Plant Records for Sawflies and Woodwasps (Hymenoptera, Symphyta) of Japan IX

Fig. 4.ɹArmitarsus watanabei, late-instar larva (A, B) and mature larva (C), photographed by H. Hara. A, B, Chitose, August 24, 2022; C, August 25, 2022 in captivity.

opencc-by-4.0Feb 2024View details →
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Fig. 7. Male genitalia. A–D in Taxonomic Notes and New Distribution and Host Plant Records for Sawflies and Woodwasps (Hymenoptera, Symphyta) of Japan VI

Fig. 7. Male genitalia. A–D, Euura imperfecta, Hokkaido; E–I, E. itoi. A, E–F, Genital capsule: A, ventral view (penis valve removed); E, F, dorsal and ventral views. B–D, G–I, Penis valve, lateral view (left dorsal). All photographed by Hara.

opencc-by-4.0Nov 2021View details →
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Fig. 3. A–G, L–O in Taxonomic Notes and New Distribution and Host Plant Records for Sawflies and Woodwasps (Hymenoptera, Symphyta) of Japan VI

Fig. 3. A–G, L–O, Euura imperfecta: A–B, female, Hokkaido, dorsal and ventral views; C–D, male, Hokkaido, dorsal and ventrolateral views; E–F, female, Honshu, dorsal and ventrolateral views; G, female, Honshu, ventrolateral view; L, egg, Hokkaido; M, semifinal instar larva, lateral view; N–O, final instar larva, lateral and dorsal views; M–O, Hokkaido, Bibai, 1986. H–K, Euura itoi: H–I, female, dorsal and ventrolateral views; J–K, male, dorsal and ventrolateral views. All photographed by Hara.

opencc-by-4.0Nov 2021View details →
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Fig. 1. A in Taxonomic Notes and New Distribution and Host Plant Records for Sawflies and Woodwasps (Hymenoptera, Symphyta) of Japan VI

Fig. 1. A, Late instar larva of Sterictiphora nipponica, 25. V. 2015, photographed by Ibuki. B, Phylloecus etorofensis, female, photographed by Hara. C, Dead female of Tremex apicalis on trunk of Alnus japonica, 23. V. 2021, photographed by Shinohara. D, Apethymus kunugi, female, photographed by Hara.

opencc-by-4.0Nov 2021View details →
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Fig. 11 in Taxonomic Notes and New Distribution and Host Plant Records for Sawflies and Woodwasps (Hymenoptera, Symphyta) of Japan VII

Fig. 11. Tomostethus nigritus: A–C, Female, head in anterior view, whole body in dorsal and ventral views; D, early instar larva, 25. IV. 2021; E, F, final or final feeding instar larva, 1. V. 2021. A–C, Photographed by Hara; D–F, photographed by Ibuki.

opencc-by-4.0Nov 2022View details →
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Fig. 8 in Taxonomic Notes and New Distribution and Host Plant Records for Sawflies and Woodwasps (Hymenoptera, Symphyta) of Japan VII

Fig. 8. Euura damnacanti: A, Lance; B, lancet; C, tangium of lancet; D, basal half of lamnium of lancet; E, F, male genitalia in dorsal and ventral views (penis valve removed in F); G, penis valve; H, first instar larvae and egg shells, 17. IV. 2021; I, final and semifinal instar larvae, Nakagawa, 7. V. 2015; J, mature larva, 30. IV. 2021. A–G, Photographed by Hara; H–J, photographed by Ibuki.

opencc-by-4.0Nov 2022View details →
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Fig. 7 in Taxonomic Notes and New Distribution and Host Plant Records for Sawflies and Woodwasps (Hymenoptera, Symphyta) of Japan VII

Fig. 7. Euura damnacanti: A–C, Female, head in anterior view, whole body in dorsal and ventral views; D–F, male, head in anterior view, whole body in dorsal and ventral views; G, H, mandibles, anterior and posterior views; I, J, right and left mandibles in outer view; K, apex of male abdomen in dorsal view. Photographed by Hara.

opencc-by-4.0Nov 2022View details →
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Fig. 1 in Battus polydamas (Lepidoptera: Papilionidae) uses the open-field Aristolochia sessilifolia (Piperales: Aristolochiaceae) as its host plant in Uruguayan savanna areas

Fig. 1. Consensus species distributions obtained by an ensemble forecasting of models consisting of 5 algorithms (Bioclim, Malahanobis Distance, MaxEnt, GARP, and SVM) using environmental data from occurrence points of (A) Battus polydamas and (B) Aristolochia sessilifolia.

opencc-by-4.0Jun 2015View details →
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Fig. 2 in Bagnalliella mojave (Thysanoptera: Phlaeothripidae) thrips inhabit small and isolated Yucca brevifolia (Agavaceae) host plants

Fig. 2. Number of leaf clusters on Yucca brevifolia vs. mean distance from plant to nearest Yucca schidigera or Y. brevifolia in 4 quarters. Yucca brevifolia plants are inhabited (closed circles) or uninhabited (open circles) by Bagnalliella mojave. Axes are log scales. Solid line is Y regressed on X. Dashed lines are the same regression with thrips presence or absence added as an indicator variable.

opencc-by-4.0Mar 2015View details →
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Fig. 1. a. Yucca brevifolia supporting 13 in Bagnalliella mojave (Thysanoptera: Phlaeothripidae) thrips inhabit small and isolated Yucca brevifolia (Agavaceae) host plants

Fig. 1. a. Yucca brevifolia supporting 13 leaf clusters and inhabited by Bagnalliella mojave. b. B. mojave adults and immatures on bases of young leaves at center of leaf cluster. c-f. Dorsal aspect of life stages illuminated from above: c, First-instar larva; d, Second-instar larva; e, Third instar (propupa); f, Brachypterous female mounted in euparal on slide.

opencc-by-4.0Mar 2015View details →
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Fig. 1 in Three new host plants of Edessa loxdalii (Hemiptera: Heteroptera: Pentatomidae) and notes on its rearing in the laboratory

Fig. 1. Edessa loxdalii nymph on soybean stem (a) and copulating adults on leaf of oriental raisin tree (b).

opencc-by-4.0Mar 2016View details →
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Fig. 1 in First record of Sesbania punicea (Fabales: Fabaceae) as a host plant for Chinavia hilaris (Hemiptera: Pentatomidae)

Fig. 1. Mean (± SE) number of Chinavia hilaris per Sesbania punicea plant over 3 time periods in 2014; time period 1 was from 11 through 27 Jun, time period 2 was from 30 Jun through 25 Jul, and time period 3 was from 28 Jul through 15 Aug. Young nymphs were 2nd and 3rd instars; old nymphs were 4th and 5th instars.

opencc-by-4.0Sep 2015View details →
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Feeding preference of Tuta absoluta on solanaceous host plants under field conditions

Open the record for dataset details and reuse information.

opencc-by-4.0Jun 2024View details →
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Fig. 1 in Behavioral responses of Aphis citricola (Hemiptera: Aphididae) and its natural enemy Harmonia axyridis (Coleoptera: Coccinellidae) to non-host plant volatiles

Fig. 1. Total numbers of Aphis citricola (A) and Harmonia axyridis (B) individuals from 2012 to 2015 in relation to ground cover vegetation. C + FM: catnip (Nepeta cataria) + French marigold (Tagetes patula), A + FM: ageratum (Ageratum houstonianum) + French marigold, C + A: catnip + ageratum; CK: native vegetation.

opencc-by-4.0Jun 2017View details →
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Fig. 4 in Behavioral responses of Aphis citricola (Hemiptera: Aphididae) and its natural enemy Harmonia axyridis (Coleoptera: Coccinellidae) to non-host plant volatiles

Fig. 4. Response of Aphis citricola adults to French marigold (Tagetes patula) (A) and catnip (Nepeta cataria) (B). T: Apple trees + aromatic plants; CK: apple trees only. The numbers of asterisks represent the level of significance: ** highly significant (P <0.01); * significant difference (P <0.05).

opencc-by-4.0Jun 2017View details →
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Figure 4 from: Gikonyo MW, Biondi M, Beran F (2019) Adaptation of flea beetles to Brassicaceae: host plant associations and geographic distribution of Psylliodes Latreille and Phyllotreta Chevrolat (Coleoptera, Chrysomelidae). In: Schmitt M, Chaboo CS, Biondi M (Eds) Research on Chrysomelidae 8. ZooKeys 856: 51-73. https://doi.org/10.3897/zookeys.856.33724

Figure 4 Metabolism of glucosinolates in Psylliodeschrysocephala and Phyllotretastriolata. Upon herbivory, glucosinolates are usually hydrolysed by the plant enzyme myrosinase to an unstable aglucone, which spontaneously rearranges to a toxic isothiocyanate. In the presence of plant specifier proteins, other hydrolysis products such as thiocyanates and nitriles are formed. Both flea beetle species sequester glucosinolates in their bodies, suggesting that not all glucosinolates are hydrolysed in feeding-damaged plant tissue. Sequestered glucosinolates may be activated for defensive purposes by an insect myrosinase in Ph.striolata, but not in Ps.chrysocephala. In addition, Ps.chrysocephala partially detoxifies glucosinolates by desulfation, whereas no glucosinolate sulfatase activity was found in Ph.striolata. According to a quantitative feeding study performed with Ps.chrysocephala, most ingested glucosinolates are activated, and isothiocyanates are detoxified by conjugation to glutathione. The isothiocyanate-glutathione conjugate is metabolized via the mercapturic acid pathway to several cyclic metabolites in Ps.chrysocephala adults (Beran et al. 2018). Examples of three structurally different glucosinolate side-chains are shown in the box. Beetle photos: Anna Schroll.

opencc-by-4.0Jun 2019View details →
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Supplementary material 1 from: Gikonyo MW, Biondi M, Beran F (2019) Adaptation of flea beetles to Brassicaceae: host plant associations and geographic distribution of Psylliodes Latreille and Phyllotreta Chevrolat (Coleoptera, Chrysomelidae). In: Schmitt M, Chaboo CS, Biondi M (Eds) Research on Chrysomelidae 8. ZooKeys 856: 51-73. https://doi.org/10.3897/zookeys.856.33724

: Data type: (Species, host plants, diet breadth, geographic distribution)

opencc-zeroJun 2019View details →
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Figure 2 from: Salvi D, D'Alessandro P, Biondi M (2019) Host plant associations in Western Palaearctic Longitarsus flea beetles (Chrysomelidae, Galerucinae, Alticini): a preliminary phylogenetic assessment. In: Schmitt M, Chaboo CS, Biondi M (Eds) Research on Chrysomelidae 8. ZooKeys 856: 101-114. https://doi.org/10.3897/zookeys.856.32430

Figure 2 Maximum Likelihood phylogenetic tree of 52 species of Longitarsus based on concatenated cox1 and 16S DNA sequences. Circles in correspondence of nodes represent bootstrap support (BS, upper half) and posterior probability (BPP, bottom half) from Bayesian analysis: black for BS > 90 and BPP > 0.98; grey for BS of 70–90% and BPP of 0.95–0.98; white for BS of 50–70% only for nodes supported by Bayesian analysis. Abbreviations: POL = polyphagous; ? = host plants unknown.

opencc-by-4.0Jun 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