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850 results for “Aphididae,”
Figure 8 from: Lagos-Kutz D, Favret C, Giordano R, Voegtlin D (2014) Molecular and morphological differentiation between Aphis gossypii Glover (Hemiptera, Aphididae) and related species, with particular reference to the North American Midwest. ZooKeys 459: 49-72. https://doi.org/10.3897/zookeys.459.7850
Figure 8 - Aphis species of the Aphid gossypii complex. A Apterous vivipara of Aphid gossypii on Rhamnus cathartica B Nymphs, apterous and alate viviparae of Aphid monardae on Monarda fistulosa C Apterous ovipara of Aphid monardae D Nymphs and apterous male (brownish in the center of the image) of Aphid monardae E Nymphs and alate vivipara of Aphid gossypii on Cucurbita pepo F Nymphs and apterous vivipara of and Aphid oestlundi on Oenothera biennis G Apterous vivipara (top) and apterous ovipara (bottom) of Aphid sedi on Hylotelephium telephium.
Figure 6 from: Lagos-Kutz D, Favret C, Giordano R, Voegtlin D (2014) Molecular and morphological differentiation between Aphis gossypii Glover (Hemiptera, Aphididae) and related species, with particular reference to the North American Midwest. ZooKeys 459: 49-72. https://doi.org/10.3897/zookeys.459.7850
Figure 6 - Antennal segments (II-VI) of alate viviparae A Aphid glycines B Aphid gossypii C Aphid monardae, showing distance from the base of antennal segment III to the first secondary sensorium, DBIII D Aphid nasturtii E Aphid oestlundi F Aphid sedi.
Figure 3 from: Lagos-Kutz D, Favret C, Giordano R, Voegtlin D (2014) Molecular and morphological differentiation between Aphis gossypii Glover (Hemiptera, Aphididae) and related species, with particular reference to the North American Midwest. ZooKeys 459: 49-72. https://doi.org/10.3897/zookeys.459.7850
Figure 3 - Inferred relationships using the SCP gene based on analysis with MrBayes. Support values (Posterior Probabilities) are below branches. Species names are followed by the collection locality (USA) and number of haplotypes.
Figure 5 from: Lagos-Kutz D, Favret C, Giordano R, Voegtlin D (2014) Molecular and morphological differentiation between Aphis gossypii Glover (Hemiptera, Aphididae) and related species, with particular reference to the North American Midwest. ZooKeys 459: 49-72. https://doi.org/10.3897/zookeys.459.7850
Figure 5 - Analysis of variance of morphological characters useful to discriminate Aphid gossypii, Aphid monardae, and Aphid sedi. The gray line represents the median. The gray diamond represents the means and standard deviation. A 95% level indicates a significant difference. A distance from the base of antennal segment III to the first secondary sensorium (DBIII) between Aphid gossypii and Aphid monardae B ratio of length of processus terminalis (PT) to the base of last antennal segment B between Aphid gossypii and Aphid sedi C ratio of length of siphunculi (SIPH) to the length of cauda (CA) between Aphid gossypii and Aphid sedi.
Figure 4 from: Lagos-Kutz D, Favret C, Giordano R, Voegtlin D (2014) Molecular and morphological differentiation between Aphis gossypii Glover (Hemiptera, Aphididae) and related species, with particular reference to the North American Midwest. ZooKeys 459: 49-72. https://doi.org/10.3897/zookeys.459.7850
Figure 4 - Habitus images of slide-mounted sexual morphs of A ovipara of Aphid monardae B male of Aphid monardae C ovipara of Aphid sedi, and apterous viviparae of D Aphid gossypii E Aphid gossypii F Aphid gossypii G Aphid sedi H Aphid glycines I Aphid monardae J Aphid nasturtii K Aphid oestlundi.
Figure 2 from: Lagos-Kutz D, Favret C, Giordano R, Voegtlin D (2014) Molecular and morphological differentiation between Aphis gossypii Glover (Hemiptera, Aphididae) and related species, with particular reference to the North American Midwest. ZooKeys 459: 49-72. https://doi.org/10.3897/zookeys.459.7850
Figure 2 - Cladogram inferred based on analysis of EF1-α with MrBayes. Support values (Posterior Probabilities) are below branches. Values under 0.95 are not presented. Species names are followed by collection locality, number of haplotypes and genus of host plant.
Figure 1 from: Lagos-Kutz D, Favret C, Giordano R, Voegtlin D (2014) Molecular and morphological differentiation between Aphis gossypii Glover (Hemiptera, Aphididae) and related species, with particular reference to the North American Midwest. ZooKeys 459: 49-72. https://doi.org/10.3897/zookeys.459.7850
Figure 1 - Cladogram inferred based on analysis of COI with MrBayes. Support values (Posterior Probabilities) are below branches. Values under 0.95 are not presented. Species names are followed by collection locality (USA: AL (Alabama), CO (Colorado), IA (Iowa), IL (Illinois), IN (Indiana), KS (Kansas), LA (Louisiana), MO (Missouri), MN (Minnesota), OH (Ohio), SD (South Dakota), WI (Wisconsin)), and number of haplotypes.
Figures 2-4 from: Mróz E, Depa Ł, Artchawakom T, Gorczyca J (2014) Micromyzus platycerii sp. n. (Hemiptera, Aphididae) – a new fern-feeding aphid species from Thailand. ZooKeys 456: 49-57. https://doi.org/10.3897/zookeys.456.8598
Figures 2-4 - Morphological features of apterous viviparous female of Micromyzus platycerii: 2 head and rostrum 3 tarsus of hind leg 4 cauda and apex of siphunculus.
Figure 5 from: Mróz E, Depa Ł, Artchawakom T, Gorczyca J (2014) Micromyzus platycerii sp. n. (Hemiptera, Aphididae) – a new fern-feeding aphid species from Thailand. ZooKeys 456: 49-57. https://doi.org/10.3897/zookeys.456.8598
Figure 5 - Microscopic slide of the paratype specimen – alate viviparous female of Micromyzus platycerii.
Figure 1 from: Mróz E, Depa Ł, Artchawakom T, Gorczyca J (2014) Micromyzus platycerii sp. n. (Hemiptera, Aphididae) – a new fern-feeding aphid species from Thailand. ZooKeys 456: 49-57. https://doi.org/10.3897/zookeys.456.8598
Figure 1 - Microscopic slide of the holotype specimen – apterous viviparous female of Micromyzus platycerii.
Figures 6-8 from: Mróz E, Depa Ł, Artchawakom T, Gorczyca J (2014) Micromyzus platycerii sp. n. (Hemiptera, Aphididae) – a new fern-feeding aphid species from Thailand. ZooKeys 456: 49-57. https://doi.org/10.3897/zookeys.456.8598
Figures 6-8 - Morphological features of alate viviparous female of Micromyzus platycerii: 6 head 7 3rd antennal segment 8 cauda and apex of siphunculus.
Figure 2c from: Cocuzza GEM, Di Silvestro S, Giordano R, Rapisarda C (2015) Congruence between cytochrome oxidase I (COI) and morphological data in Anuraphis spp. (Hemiptera, Aphididae) with a comparison between the utility of the 5' barcode and 3' COI regions. ZooKeys 529: 123-144. https://doi.org/10.3897/zookeys.529.6081
Figure 2c - MrBayes tree estimated using 648 bp at the 3' end of COI for selected Anuraphis species.
Figure 2d from: Cocuzza GEM, Di Silvestro S, Giordano R, Rapisarda C (2015) Congruence between cytochrome oxidase I (COI) and morphological data in Anuraphis spp. (Hemiptera, Aphididae) with a comparison between the utility of the 5' barcode and 3' COI regions. ZooKeys 529: 123-144. https://doi.org/10.3897/zookeys.529.6081
Figure 2d - MrBayes tree estimated using 658 bp at the 5' end of COI for selected Anuraphis species.
Figure 43 from: Jiang L-Y, Chen J, Qiao G-X (2015) A new species of Mollitrichosiphum Suenaga from Taiwan Island (Hemiptera, Aphididae), based on morphological characteristics and DNA sequences. ZooKeys 524: 45-63. https://doi.org/10.3897/zookeys.524.6075
Figure 43 - Neighbour-joining tree for Mollitrichosiphum samples based on Cytb sequences. Numbers above branches indicate bootstrap values (>50%).
Figures 27-37 from: Jiang L-Y, Chen J, Qiao G-X (2015) A new species of Mollitrichosiphum Suenaga from Taiwan Island (Hemiptera, Aphididae), based on morphological characteristics and DNA sequences. ZooKeys 524: 45-63. https://doi.org/10.3897/zookeys.524.6075
Figures 27-37 - Mollitrichosiphum tumorisiphum Qiao & Jiang, sp. n. Alate viviparous female: 27 dorsal view of body 28 dorsal view of head 29 antennal segments I–IV 30 antennal segments V–VI 31 ultimate rostral segment 32 hind tibia, tarsi and claws 33 spinules on venter of abdominal segment V 34 siphunculus 35 cauda and anal plate 36 genital plate. Second instar larva: 37. dorsal view of body. Scale bars = 0.10 mm.
Figures 1-12 from: Jiang L-Y, Chen J, Qiao G-X (2015) A new species of Mollitrichosiphum Suenaga from Taiwan Island (Hemiptera, Aphididae), based on morphological characteristics and DNA sequences. ZooKeys 524: 45-63. https://doi.org/10.3897/zookeys.524.6075
Figures 1-12 - Mollitrichosiphum tumorisiphum Qiao & Jiang, sp. n. Apterous viviparous female: 1 dorsal view of head 2 antenna 3 ultimate rostral segment 4 mesosternal furca 5 hind tibia 6 dorsal seta on abdominal tergite I 7 spinules on venter of abdominal segment V 8 siphunculus 9 cauda 10 anal plate 11 genital plate. Alate viviparous female: 12. antennal segment III. Scale bars = 0.10 mm.
Figure 42 from: Jiang L-Y, Chen J, Qiao G-X (2015) A new species of Mollitrichosiphum Suenaga from Taiwan Island (Hemiptera, Aphididae), based on morphological characteristics and DNA sequences. ZooKeys 524: 45-63. https://doi.org/10.3897/zookeys.524.6075
Figure 42 - Neighbour-joining tree for Mollitrichosiphum samples based on COI sequences. Numbers above branches indicate bootstrap values (>50%).
Figure 1a from: Cocuzza GEM, Di Silvestro S, Giordano R, Rapisarda C (2015) Congruence between cytochrome oxidase I (COI) and morphological data in Anuraphis spp. (Hemiptera, Aphididae) with a comparison between the utility of the 5' barcode and 3' COI regions. ZooKeys 529: 123-144. https://doi.org/10.3897/zookeys.529.6081
Figure 1a - Neighbor-Joining tree showing relationships among selected Anuraphis species estimated using 648 bp at the 3' end of the COI mitochondrial gene. Distance were estimated using the p-distance model of sequence evolution.
Figure 2b from: Cocuzza GEM, Di Silvestro S, Giordano R, Rapisarda C (2015) Congruence between cytochrome oxidase I (COI) and morphological data in Anuraphis spp. (Hemiptera, Aphididae) with a comparison between the utility of the 5' barcode and 3' COI regions. ZooKeys 529: 123-144. https://doi.org/10.3897/zookeys.529.6081
Figure 2b - Likelihood tree estimated using 658 bp at the 5' end of COI for selected Anuraphis species.
Figure 2a from: Cocuzza GEM, Di Silvestro S, Giordano R, Rapisarda C (2015) Congruence between cytochrome oxidase I (COI) and morphological data in Anuraphis spp. (Hemiptera, Aphididae) with a comparison between the utility of the 5' barcode and 3' COI regions. ZooKeys 529: 123-144. https://doi.org/10.3897/zookeys.529.6081
Figure 2a - Likelihood tree estimated using 648 bp at the 3' end of COI for selected Anuraphis species.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
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DANDI Archive for NWB datasets
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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.