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FIGURE 11 in A new species of Metopeurum Mordvilko, 1914 (Hemiptera: Aphididae) from the Transcaucasus, with a key to the species of this genus
FIGURE 11. Map with sampling sites of Metopeurum caucasicum sp. nov. 1. Armenia, Hankavan (083E22); 2. Armenia, Artavaz (026E21); 3. Georgia, near Gveleti waterfall (TA–T–143); 4. Armenia, Megradzor (089E22); 5. Semenovka (142E23); 6. Semenovka (135E23); 7. Semenovka (133E23).
FIGURE 2 in The species of Uroleucon (Hemiptera: Aphididae) living on Adesmia (Fabaceae) in Argentina, with the description of a new species
FIGURE 2. Unrooted neighbor-joining dendrogram of selected South American native Uroleucon species (see Table 1) and Northern Hemisphere Uroleucon species, derived from Tamura-Nei distances calculated from mitochondrial tRNAleu-COII sequences (Table 3).
FIGURE 1 in The species of Uroleucon (Hemiptera: Aphididae) living on Adesmia (Fabaceae) in Argentina, with the description of a new species
FIGURE 1. Uroleucon nahuelhuapense Nieto Nafría & von Dohlen, sp. n. Apterous viviparous female. A, habitus. B, Antennal segments II and III. C, Antennal segment VI and very end of antennal segment V. D, Tarsus and very end of tibia of hind leg. E, Siphunculus. F, Apical part of siphunculus. G, cauda and anal plate. A–C, F and G, holotype; D and E, a paratype, specimen number 5.
FIGURE 1 in Description of the previously unknown morphs of Periphyllus koelreuteriae (Takahashi) (Hemiptera, Aphididae: Chaitophorinae)
FIGURE 1. Periphyllus koelreuteriae—apterous viviparous female: (a) general view, (b) antenna, (c) apical segment of rostrum, (d) hind tarsus, (e) siphunculus, (f) cauda.
FIGURE 3 in Description of the previously unknown morphs of Periphyllus koelreuteriae (Takahashi) (Hemiptera, Aphididae: Chaitophorinae)
FIGURE 3. Periphyllus koelreuteriae—alate male: (a) head, (b) antenna, (c) apical segment of rostrum, (d) hind tarsus, (e) fore wing, (f) abdomen, (g) siphunculus, (h) cauda, (i) genitalia.
FIGURE 2 in Description of the previously unknown morphs of Periphyllus koelreuteriae (Takahashi) (Hemiptera, Aphididae: Chaitophorinae)
FIGURE 2. Periphyllus koelreuteriae—oviparous female: (a) general view, (b) antenna, (c) apical segment of rostrum, (d) hind tibia with pseudosensoria and tarsus, (e) siphunculus, (f) cauda.
FIGURES 1–4 in A new Brazilian species of Harpasus Mulsant (Coleoptera, Coccinellidae, Chilocorinae), a predator of Tinocallis kahawaluokalani (Kirkaldy) (Hemiptera, Aphididae)
FIGURES 1–4. Habitus of Harpasus aureus Almeida & Carvalho sp.n.; 1, dorsal view; 2, frontal view; 3, lateral view; 4, ventral view.
FIGURE 7 in Three new species of the genus Neuquenaphis (Hemiptera, Aphididae, Spicaphidinae) from southernmost South America
FIGURE 7. Neighbor-joining dendrograms for Neuquenaphis samples sequenced in this study; A, Dendrogram based on Kimura 2-parameter distances for the COI barcode locus; B, Dendrogram based on Tamura-Nei distances for the tRNA-COII locus. We were unable to obtain tRNA-COII sequences for other samples with established COI sequences. NOTE: each species name is followed by the number of the sample to which the analysed specimens belong, which begins with CHI, and in parentheses by the GenBank accession number. Sample data in legend of Table 3.
FIGURE 4 in Three new species of the genus Neuquenaphis (Hemiptera, Aphididae, Spicaphidinae) from southernmost South America
FIGURE 4. Neuquenaphis aurata sp. n.; A–I, apterous viviparous female. A, antero-cephalic finger-shaped process. B, postero-cephalic finger-shaped process. C, D, prothoracic pleural and submarginal processes, respectively. E, prothoracic postero-lateral bulge. F, apex of antennal segment V and proximal part of antennal segment VI. G, finger-shaped process on abdominal segment 7. H, siphunculus. I, cauda. J–Q, alate viviparous female. J, anterior cephalic short finger-shaped process. K, prothoracic postero-lateral slight bulge, with seta. L, marginal short rod-shaped process on abdominal segment 3. M, submarginal tubercle on abdominal segment 3. N, spinal rod-shaped process on abdominal segment 2. O, middle portion of antennal segment III, with secondary sensoria. P, siphunculus. Q, cauda. NOTE: The scales vary according to pieces drawn; see the range of measurements in Table 2.
FIGURE 2 in Three new species of the genus Neuquenaphis (Hemiptera, Aphididae, Spicaphidinae) from southernmost South America
FIGURE 2. Neuquenaphis blackmani sp. n. A–H, apterous viviparous female. A, antero-cephalic finger-shaped process. B, prothoracic submarginal wart-shaped process. C, prothoracic marginal wart-shaped process. D, prothoracic posterolateral seta. E, finger-shaped process on abdominal segment 8. F, proximal part of antennal segment VI. G, siphunculus. H, cauda. I–V, alate viviparous female. I, anterior cephalic tubercle. J, K, spinal rod-shaped process on abdominal segments 2 and 3, respectively. L, M, marginal and submarginal, respectively, rod-shaped process on abdominal segment 4. O, P, spinal and marginal, respectively, conical-shaped tubercle on abdominal segment 7. Q, R, abdominal seated setae. S, rod-shaped process on abdominal segments 8. T, middle portion of antennal segment III, with secondary sensoria. U, siphunculus. V, cauda. NOTE: The scales vary according to pieces drawn; see the range of measurements in Table 2.
FIGURE 3 in Aphis (Hemiptera, Aphididae) species living on Baccharis (Asteraceae) in southern South America, with description of three new species
FIGURE 3. Aphis fuentesi Nieto Nafría & Ortego, sp. n. A–D apterous viviparous females; A, specimen moderately sclerotized; B, specimen extensively sclerotized; C, dorso-abdominal reticulation; D, siphunculus and marginal tubercles on abdominal segments 6 and 7. F–G, alate viviparous females; F, habitus; G, antennal segment III. H, oviparous female. I, male. The scales vary according to specimens or parts photographed; see measurements in Table 2.
FIGURE 1 in Aphis (Hemiptera, Aphididae) species living on Baccharis (Asteraceae) in southern South America, with description of three new species
FIGURE 1. Aphis ingeborgae Nieto Nafría & Brown, sp. n. A–G, apterous viviparous females; A, specimen extensively sclerotized; B, specimen moderately sclerotized; C, dorso-cephalic reticulation; D, dorso-abdominal reticulation; E, prothoracic marginal tubercle; F, three different marginal tubercles on abdominal segment 1; G, marginal tubercle on an intermediate abdominal segment. H–I, alate viviparous female; H, habitus; I, antennal segment III. The scales vary according to specimens or parts photographed; see measurements in Table 1.
FIGURE 2 in Aphis (Hemiptera, Aphididae) species living on Baccharis (Asteraceae) in southern South America, with description of three new species
FIGURE 2. Aphis conspicua Nieto Nafría & Mier Durante, sp. n. A–D, apterous viviparous female; A, specimen with intermediate dorsal sclerotisation; B, dorso-thoracic reticulation; C, marginal tubercles on metathorax (small one placed partially on the pigmented sclerite) and abdominal segments 1, 2 and 3; D, dorso-abdominal reticulation. E–F, Alate viviparous females; E, head plus a part of prothorax, and a part of metathorax plus abdomen; F, antennal segment III. The scales vary according to specimens or parts photographed; see measurements in Table 1.
FIGURE 5–8 in A new species of Aphidura Hille Ris Lambers, and additional data for Aphidura pakistanensis (Hemiptera: Aphididae) from Republic of Georgia
FIGURE 5–8. Aphidura pakistanensis Nieto Nafría, Mier Durante & Remaudière, 2013 from Georgia. 5. Habitus of apterous viviparous female (bar: 500 μm); Alate viviparous female. 6. ANT IV–VI (bar: 100 μm); 7. Head with ANT I–III (bar: 200 μm); 8. Habitus (bar: 500 μm).
FIGURES 1–4 in A new species of Aphidura Hille Ris Lambers, and additional data for Aphidura pakistanensis (Hemiptera: Aphididae) from Republic of Georgia
FIGURES 1–4. Aphidura jimoi sp. nov. Apterous viviparous female, holotype. 1. ANT (bar: 100 μm); 2. Anterior part of body (bar: 200 μm); 3. Posterior part of abdomen with SIPH and cauda (bar: 100 μm); 4. Habitus (bar: 500 μm).
Fig. 12 in First record of Myzus (Nectarosiphon) persicae (Sulzer, 1776) (Hemiptera: Aphididae) occuring on Valeriana fauriei (Caprifoliaceae)
Fig. 12. Morphs of two M. persicae populations reared on buckwheat plants (15 °C, 10L:14D) over four generations (Gen — generation of the single adult viviparous female initially transferred on buckwheat at maintained (15 °C, 10L:14D) was defined as the first generation; N — population from Nayoro; P — population from Pippu; rep — replication; APT — apterous viviparous female; ALT — alate viviparous female). Рис. 12. Морфы двух популЯций M. persicae, выраЩенных на растениЯх гречихи (15 °C, 10L:14D), в течение четырёх поколений (Gen — поколение единственной вЗрослой живородЯЩей самки, первоначально перенесённоq на гречиху (15 °C, 10L:14D), было принЯто как первое поколение; N — популЯциЯ иЗ Наёро; P — популЯциЯ иЗ Пиппу; rep — раЗмножение; APT — бескрылаЯ живородЯЩаЯ самка; ALT — крылатаЯ живородЯЩаЯ самка).
Figs 10–11 in First record of Myzus (Nectarosiphon) persicae (Sulzer, 1776) (Hemiptera: Aphididae) occuring on Valeriana fauriei (Caprifoliaceae)
Figs 10–11. Myzus persicae collected from Valeriana fauriei: 10 — adult apterous viviparous female (specimen number: 37098); 11 — alate viviparous female (specimen number: 38011). Scale bars: 1 mm. Рис. 10–11. Myzus persicae собраннаЯ с Valeriana fauriei: 10 — вЗрослаЯ бескрылаЯ живородЯЩаЯ самка (номер ЭкЗемплЯра: 37098); 11 — крылатаЯ живородЯЩаЯ самка (номер ЭкЗемплЯра: 38011). МасШтабные линейки: 1 мм.
Figs 1–9 in First record of Myzus (Nectarosiphon) persicae (Sulzer, 1776) (Hemiptera: Aphididae) occuring on Valeriana fauriei (Caprifoliaceae)
Figs 1–9. Valeriana fauriei plant, Myzus persicae occurring on the plant, and plant damage caused by the aphid: 1 — nursery plant of V. fauriei; 2 — colony infesting the plant part near the growing point; 3 — adult apterous viviparous female; 4 — colony infesting the underside of a lower leaf; 5–6 — adult apterous viviparous females; 7 — alate viviparous female; 8 — smearing of the upper side of a lower leaf with honeydew and exuviae produced by the aphids; 9 — withered the leaves of V. fauriei; 1–3 — Nayoro (April 2020); 4–7 — Pippu (December 2020); 8–9 — Pippu (November 2020). Рис. 1–9. Valeriana fauriei, Myzus persicae и повреждениЯ, выЗванные тлёй: 1 — саженцы V. fauriei; 2 — колониЯ, поражаюЩаЯ часть растениЯ рЯдом с точкой роста; 3 — вЗрослаЯ бескрылаЯ живородЯЩаЯ самка; 4 — колониЯ, поражаюЩаЯ нижнюю часть нижнего листа; 5–6 — вЗрослые бескрылые живородЯЩие самки; 7 — крылатаЯ живородЯЩаЯ самка; 8 — верхнЯЯ сторона нижнего листа, ЗагрЯЗнённаЯ медвЯной росой и ЭкЗувиЯ тлей; 9 — увЯдШие листьЯ V. fauriei; 1–3 — Наёро (апрель 2020 г.); 4–7 — Пиппу (декабрь 2020 г.); 8–9 — Пиппу (ноЯбрь 2020 г.).
Fig. 3 in Phylogenetic relationships of Dysaphis pyri (Boyer de Fonscolombe) and Dysaphis reaumuri (Mordvilko) (Hemiptera, Sternorrhyncha: Aphididae): COI and EF-1α evidence
Fig. 3 BI tree showing phylogenetic relationships among D. pyri, D. reaumuri and other congeneric species with two outgroup species, A. gossypii and T. citricida, based on partial sequences of nuclear elongation factor 1 alpha (EF- 1α; 489 positions in final set). Numbers above branches indicate support of MP (left) and ML (right) bootstrap test with 1,000 replicates, and numbers below branches indicate posterior probabilities of BI analysis. Sample acronyms as in Table 1
Fig. 2 in Phylogenetic relationships of Dysaphis pyri (Boyer de Fonscolombe) and Dysaphis reaumuri (Mordvilko) (Hemiptera, Sternorrhyncha: Aphididae): COI and EF-1α evidence
Fig. 2 Bayesian inference (BI) tree showing phylogenetic relationships among Dysaphis pyri, Dysaphis reaumuri and other congeneric species with two outgroup species, Aphis gossypii and Toxoptera citricida, based on partial sequences of mitochondrial cytochrome oxidase subunit I (COI; 217 positions in final set). Numbers above branches indicate support of maximum parsimony (MP; left) and maximum likelihood (ML; right) bootstrap test with 1,000 replicates, and numbers below branches indicate posterior probabilities of BI analysis. Sample acronyms as in Table 1
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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.
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.