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850 results for “Aphididae,”

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zenodo28/100

Figure 1 from: Barjadze S, Jensen AS, Kanturski M (2018) Ericaphis voegtlini, a new, unusual aphid species from the USA (Hemiptera, Aphididae). ZooKeys 785: 133-143. https://doi.org/10.3897/zookeys.785.28006

Figure 1 Ericaphisvoegtlini sp. n. General view. a Apterous viviparous female b Alate viviparous female.

opencc-by-4.0Sep 2018View details →
zenodo28/100

Figure 4 from: Barjadze S, Jensen AS, Kanturski M (2018) Ericaphis voegtlini, a new, unusual aphid species from the USA (Hemiptera, Aphididae). ZooKeys 785: 133-143. https://doi.org/10.3897/zookeys.785.28006

Figure 4 Alate viviparous female of Ericaphisvoegtlini sp. n. Characters. a Head bANT III with secondary rhinaria c Structure of the sensoria with visible fibriation (arrow) d Hind tarsus e Abdominal sclerotisation f Marginal tubercles on ABD VII and ABD VIII.

opencc-by-4.0Sep 2018View details →
zenodo28/100

Figure 2 from: Cameron SA, Corbet SA, Whitfield JB (2019) Bumble bees (Hymenoptera: Apidae: Bombus terrestris) collecting honeydew from the giant willow aphid (Hemiptera: Aphididae). Journal of Hymenoptera Research 68: 75-83. https://doi.org/10.3897/jhr.68.30495

Figure 2 - A Diurnal changes in total numbers of bees (blue dots) and wasps (red squares) B solute concentration in fresh honeydew (diamonds) and bumble bee crop contents (red dots). Arrows show times of sunrise and sunset.

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

Figure 1 from: Cameron SA, Corbet SA, Whitfield JB (2019) Bumble bees (Hymenoptera: Apidae: Bombus terrestris) collecting honeydew from the giant willow aphid (Hemiptera: Aphididae). Journal of Hymenoptera Research 68: 75-83. https://doi.org/10.3897/jhr.68.30495

Figure 1 - A Giant willow aphids ( Tuberolachnus salignus ) on a branch of Salix alba ; larger aphids range from 5.1–5.7 mm B Bombus terrestris collecting honeydew from leaf litter beneath several branches bearing the aphids C holding a plastic plate beneath the aphid colonies to collect honeydew droplets D collecting honeydew droplets from the plate using a 5 μl glass capillary tube E compressing a worker bumble bee to force regurgitation of crop contents onto the plate F using a refractometer to measure solute concentration of honeydew.

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

Figure 3 from: Li Q, Yao J, Zeng L, Lin X, Huang X (2019) Molecular and morphological evidence for the identity of two nominal species of Astegopteryx (Hemiptera, Aphididae, Hormaphidinae). ZooKeys 833: 59-74. https://doi.org/10.3897/zookeys.833.30592

Figure 3 Photographs of live specimens showing high morphological variation among samples. Based on specimen voucher number, these photographs correspond to the following sequences in the phylogenetic trees; 1 HL20170205_7 2 HL20170606_8 3 HL20170409_2 4 HL20170403_13 5 HL20170226_3 6 HL20150416_14 7 HL20160417_7 8 HL20161004_1 9 HL20161228_18 10 HL20150530_4 11 HL20160326_4 12 HL20170403_10 13 HL20160131_8 14 HL20160512_1 15 HL20170318_3 16 HL20170419_4 17 HL20170926_23 18 HL20160217_1 19 HLzld20171102_15 20 HLzld20171103_22 21 HLzld20171108_6 22 HLzld20171108_7 23 HLzld20171111_3 24 HLzld20171126_6 25 HL20170205_8 26 HL20170806_1 27 HL20160412_5 28 HLzld20171102_16.

opencc-by-4.0Apr 2019View details →
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Figure 2 from: Li Q, Yao J, Zeng L, Lin X, Huang X (2019) Molecular and morphological evidence for the identity of two nominal species of Astegopteryx (Hemiptera, Aphididae, Hormaphidinae). ZooKeys 833: 59-74. https://doi.org/10.3897/zookeys.833.30592

Figure 2 Haplotype networks based on COI sequences. The circles represent different haplotypes, while different colors correspond to the geographical origins of samples and sizes represent relative numbers of sequences (H_1: 23; H_2: 1; H_3: 2; H_4: 3; H_5: 7; H_6: 3; H_7: 3; H_8: 1; H_9: 1; H_10: 1). The short line segments indicate mutated positions between haplotypes.

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

Figure 1 from: Li Q, Yao J, Zeng L, Lin X, Huang X (2019) Molecular and morphological evidence for the identity of two nominal species of Astegopteryx (Hemiptera, Aphididae, Hormaphidinae). ZooKeys 833: 59-74. https://doi.org/10.3897/zookeys.833.30592

Figure 1 The Neighbor-joining (NJ) trees based on COI (A), Cytb (B), EF-1α (C), tRNA/COII (D), and the combined data of all four genes (E). The ingroup specimens are printed in bold and the bootstrap values higher than 50 are indicated. The sequences are named as putative species name plus specimen voucher number.

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

Supplementary material 2 from: Li Q, Yao J, Zeng L, Lin X, Huang X (2019) Molecular and morphological evidence for the identity of two nominal species of Astegopteryx (Hemiptera, Aphididae, Hormaphidinae). ZooKeys 833: 59-74. https://doi.org/10.3897/zookeys.833.30592

: Data type: molecular data

opencc-zeroApr 2019View details →
zenodo28/100

Supplementary material 1 from: Li Q, Yao J, Zeng L, Lin X, Huang X (2019) Molecular and morphological evidence for the identity of two nominal species of Astegopteryx (Hemiptera, Aphididae, Hormaphidinae). ZooKeys 833: 59-74. https://doi.org/10.3897/zookeys.833.30592

: Data type: molecular data

opencc-zeroApr 2019View details →
zenodo28/100

FIGURE 3 in Three new species of the genus Neuquenaphis (Hemiptera, Aphididae, Spicaphidinae) from southernmost South America

FIGURE 3. Neuquenaphis aurata sp. n. A, apterous viviparous female. B, alate viviparous female.

opennotspecifiedApr 2019View details →
zenodo28/100

FIGURE 1 in Three new species of the genus Neuquenaphis (Hemiptera, Aphididae, Spicaphidinae) from southernmost South America

FIGURE 1. Neuquenaphis blackmani sp. n. A, apterous viviparous female. B, alate viviparous female.

opennotspecifiedApr 2019View details →
zenodo28/100

FIGURE 4 in Description of the previously unknown morphs of Periphyllus koelreuteriae (Takahashi) (Hemiptera, Aphididae: Chaitophorinae)

FIGURE 4. Distribution of Periphyllus koelreuteriae.

opennotspecifiedApr 2019View details →
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Figure 5 from: Zúñiga-Centeno A, Sandoval-Carvajal I, Montero-Astúa M, Villalobos-Muller W, Quốc NB, Pérez Hidalgo N (2019) A molecular study of Neophyllaphis varicolor (Hemiptera, Aphididae) in Costa Rica. ZooKeys 865: 123-135. https://doi.org/10.3897/zookeys.865.35213

Figure 5 Phylogenetic analysis of Neophyllaphisaraucariae Takahashi, Neophyllaphispodocarpi Takahashi and Neophyllaphisvaricolor Miller & Halbert, using concatenated sequences of cytochrome c oxidase subunit I and elongation factor 1α made by Bayesian inference and using as outgroup Greenideapsidii van der Goot. and Greenideaanonae (Pergande). Sample names: species name - colony code - (a, b or c represent the specimen sampled) - country code. Key: CHN: China, CRI: Costa Rica, ESP: Spain, USA: United States, VNM: Vietnam. Scale bar represents 0.03 changes per site.

opencc-by-4.0Oct 2019View details →
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Figure 3 from: Zúñiga-Centeno A, Sandoval-Carvajal I, Montero-Astúa M, Villalobos-Muller W, Quốc NB, Pérez Hidalgo N (2019) A molecular study of Neophyllaphis varicolor (Hemiptera, Aphididae) in Costa Rica. ZooKeys 865: 123-135. https://doi.org/10.3897/zookeys.865.35213

Figure 3 Neophyllaphisvaricolor Miller & Halbert, alate A alate aphid B head C antennal segment III and D abdomen.

opencc-by-4.0Oct 2019View details →
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Figure 2 from: Zúñiga-Centeno A, Sandoval-Carvajal I, Montero-Astúa M, Villalobos-Muller W, Quốc NB, Pérez Hidalgo N (2019) A molecular study of Neophyllaphis varicolor (Hemiptera, Aphididae) in Costa Rica. ZooKeys 865: 123-135. https://doi.org/10.3897/zookeys.865.35213

Figure 2 Neophyllaphisvaricolor Miller & Halbert, apterous A body B anterior part of the body C antennae, and D posterior part of body.

opencc-by-4.0Oct 2019View details →
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Figure 4 from: Zúñiga-Centeno A, Sandoval-Carvajal I, Montero-Astúa M, Villalobos-Muller W, Quốc NB, Pérez Hidalgo N (2019) A molecular study of Neophyllaphis varicolor (Hemiptera, Aphididae) in Costa Rica. ZooKeys 865: 123-135. https://doi.org/10.3897/zookeys.865.35213

Figure 4 Phylogenetic analysis of Neophyllaphisaraucariae Takahashi, Neophyllaphisbrimblecombei Carver, Neophyllaphispodocarpi Takahashi, Neophyllaphistotarae Cottier, and Neophyllaphisvaricolor Miller & Halbert, using sequences of cytochrome c oxidase subunit I, made with Bayesian inference and using as outgroup Greenideapsidii van der Goot. and Greenideaanonae (Pergande). Sequence codes: species name - colony code - (a, b or c represent the specimen sampled) - country code. Key: AUS: Australia, CHN: China, CRI: Costa Rica, ESP: Spain, JPN: Japan, NZL: New Zealand, USA: United States, VNM: Vietnam. Scale bar represents 0.03 changes per site.

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

Figure 1 from: Zúñiga-Centeno A, Sandoval-Carvajal I, Montero-Astúa M, Villalobos-Muller W, Quốc NB, Pérez Hidalgo N (2019) A molecular study of Neophyllaphis varicolor (Hemiptera, Aphididae) in Costa Rica. ZooKeys 865: 123-135. https://doi.org/10.3897/zookeys.865.35213

Figure 1 ANeophyllaphisvaricolor Miller & Halbert, apterous individuals from Costa Rica BPodocarpuschinensis Wall. ex J.Forbes, and CPodocarpusfalcatus (Thunb.) Mirb.

opencc-by-4.0Oct 2019View details →
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Figure 3 in Orientation of Hippodamia variegata (Coleoptera: Coccinellidae) to healthy and Beauveria bassiana-infected Aphis fabae (Hemiptera: Aphididae) in an olfactometer system

Figure 3. Response of Hippodamia variegata to broad bean plants infested by A. fabae infected by Beauveria bassiana at the interval of 24 h after infection versus broad bean plants infested by A. fabae infected by B. bassiana at intervals of 48 (a) and 72 (b) h after infection. The white bars indicate the numbers of insects choosing broad bean plants infested by A. fabae infected by B. bassiana at intervals 48 and 72 h after infection, whereas the black bars indicate the numbers of insects that chose broad bean plants infested by A. fabae infected by B. bassiana at the interval of 24 h after infection.

opencc-by-4.0Jan 2015View details →
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Figure 2 in Is the subfamily Eriosomatinae (Hemiptera: Aphididae) monophyletic?

Figure 2. The strict consensus tree of the 14 MPTs from the MP analysis combining sequences from 2 mitochondrial genes (COI and COII) and 2 nuclear genes (EF-1α and LWO). Note that the topologies of the MPTs were almost identical.

opencc-by-4.0Mar 2014View details →
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Figure 3. A neighbor joining tree using cytochrome c oxidase subunit 1 in DNA barcoding of black cherry aphid Myzus cerasi (Fabricus, 1775) (Hemiptera: Aphididae) populations collected from Prunus avium and Prunus cerasus

Figure 3. A neighbor joining tree using cytochrome c oxidase subunit 1 sequences from Myzus cerasi populations.

opencc-by-4.0Jan 2020View details →

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Allen Brain Atlas

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Last verified 2026-04-30Open record

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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