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850 results for “Aphididae,”
Figures 1-11 from: Qiao G, Zhang B, Lou Y (2013) A new genus and species of Macrosiphini (Hemiptera, Aphididae) from China, living on Isodon eriocalyx. ZooKeys 359: 1-12. https://doi.org/10.3897/zookeys.359.6219
Figures 1-11 - Nigritergaphis crassisetosa sp. n. Apterous viviparous female: 1 dorsal view of head 2 antennal segments I–IV 3 antennal segments V–VI 4 ultimate rostral segment 5 mesosternal furca 6, 7 siphunculi 8 cauda 9 anal plate 10 hind tarsal segment 11 genital plate.
Figures 18-28 from: Qiao G, Zhang B, Lou Y (2013) A new genus and species of Macrosiphini (Hemiptera, Aphididae) from China, living on Isodon eriocalyx. ZooKeys 359: 1-12. https://doi.org/10.3897/zookeys.359.6219
Figures 18-28 - Nigritergaphis crassisetosa sp. n. Apterous viviparous female: 18 dorsal view of body 19 dorsal view of head 20 antennal segments I–VI 21 ultimate rostral segment 22 mesosternal furca 23, 24 siphunculi 25 cauda 26 anal plate 27 hind tarsal segment 28 genital plate.
Figure 4 from: Rakauskas R, Havelka J, Zaremba A, Bernotienė R (2014) Mitochondrial COI and morphological evidence for host specificity of the black cherry aphids Myzus cerasi (Fabricius, 1775) collected from different cherry tree species in Europe (Hemiptera, Aphididae). ZooKeys 388: 1-15. https://doi.org/10.3897/zookeys.388.7034
Figure 4 - Plot of the mean scores of the individual LDF values (number of specimens per sample is given in Table 1) plotted against the mean body length for 30 samples of Myzus cerasi (normal font in Table 1) used to evaluate effectiveness of the eventual identification key. The icons are color-coded to match the COI haplotypes. Samples cluster in accordance with winter host plant and COI haplotype (haplotype number is given in parentheses, see Table 2 for haplotype information).
Figure 1 from: Rakauskas R, Havelka J, Zaremba A, Bernotienė R (2014) Mitochondrial COI and morphological evidence for host specificity of the black cherry aphids Myzus cerasi (Fabricius, 1775) collected from different cherry tree species in Europe (Hemiptera, Aphididae). ZooKeys 388: 1-15. https://doi.org/10.3897/zookeys.388.7034
Figure 1 - Haplotype network (TCS 1.21 software: Clement et al. 2000) for COI fragment (616 positions in final set) haplotypes of Myzus cerasi and Myzus borealis. The haplotype with the highest outgroup probability is displayed as a square, while others are displayed as ovals. For sample information, see Table 2.
Figure 3 from: Rakauskas R, Havelka J, Zaremba A, Bernotienė R (2014) Mitochondrial COI and morphological evidence for host specificity of the black cherry aphids Myzus cerasi (Fabricius, 1775) collected from different cherry tree species in Europe (Hemiptera, Aphididae). ZooKeys 388: 1-15. https://doi.org/10.3897/zookeys.388.7034
Figure 3 - Plot of the mean scores of the first two canonical variates for 20 samples of Myzus cerasi (for specimen numbers per sample see Table 1). Samples cluster in accordance with winter host plant and COI haplotype (haplotype number is given in parentheses, see Table 2 for other haplotypes).
Figure 2 from: Rakauskas R, Havelka J, Zaremba A, Bernotienė R (2014) Mitochondrial COI and morphological evidence for host specificity of the black cherry aphids Myzus cerasi (Fabricius, 1775) collected from different cherry tree species in Europe (Hemiptera, Aphididae). ZooKeys 388: 1-15. https://doi.org/10.3897/zookeys.388.7034
Figure 2 - Maximum likelihood (ML) tree showing phylogenetic relationships among Myzus cerasi based on partial sequences of mitochondrial COI (616 positions in final set). Numbers above branches indicate support of NJ (left, > 50%) and MP (right, > 50%) bootstrap test with 1000 replicates, and numbers below branches indicate support of ML (left, > 50%) bootstrap test with 1000 replicates and posterior probabilities of BI analysis (right, > 0.50). Samples used for the discriminant analysis with a priori specified group membership followed by the construction of identification key are asterisked (*). The remaining samples were used for the post hoc classification. Sample numbers are the same as given in Table 1, together with the abbreviated symbol of respective country BG – Bulgaria, BY – Belarus, D – Germany, HU – Hungary, IT – Italy, LV – Latvia, LT – Lithuania, PL – Poland, RO – Romania, TR – Turkey, UA – Ukraine.
Figures 4-11 from: Miller G, Jensen A, Metz M, Parmenter R (2014) A new species of Atheroides Haliday (Hemiptera, Aphididae) native to North America. ZooKeys 452: 35-50. https://doi.org/10.3897/zookeys.452.8089
Figures 4-11 - Atheroides vallescaldera n. sp. 4 holotype habitus (Left side focal planes from dorsum to middle. Right side focal planes from middle to ventral surface.) 5 antenna of apterous vivipara 6 head (left half dorsal, right half ventral) 7 ultimate rostral segments 8 examples of dorsal abdominal setae variation 9 tergite VIII (dorsal) 10 empodial setae 11 anal and genital figs. (Scale indicated by 0.20 mm measure bars and corresponding figure number.).
Figure 3 from: Miller G, Jensen A, Metz M, Parmenter R (2014) A new species of Atheroides Haliday (Hemiptera, Aphididae) native to North America. ZooKeys 452: 35-50. https://doi.org/10.3897/zookeys.452.8089
Figure 3 - Single, most parsimonious tree of 14 steps (CI=85, RI=88) resulting from an exhaustive search in TNT. Closed circles indicate unique forward changes. Open circles indicate either forward changes with homoplasy or reversals. Numbers on nodes in squares indicate Bremer support values for that node.
Figure 2 from: Miller G, Jensen A, Metz M, Parmenter R (2014) A new species of Atheroides Haliday (Hemiptera, Aphididae) native to North America. ZooKeys 452: 35-50. https://doi.org/10.3897/zookeys.452.8089
Figure 2 - Second author in the habitat of the type locality for the new species along Santa Rosa Creek.
Figure 1 from: Miller G, Jensen A, Metz M, Parmenter R (2014) A new species of Atheroides Haliday (Hemiptera, Aphididae) native to North America. ZooKeys 452: 35-50. https://doi.org/10.3897/zookeys.452.8089
Figure 1 - Map of the Valles Caldera National Preserve, New Mexico, USA, showing collection location.
Figure 1 from: Kanturski M, Wieczorek K (2014) Systematic position of Eulachnus cembrae Börner with description of hitherto unknown sexual morphs of E. pumilae Inouye (Hemiptera, Aphididae, Lachninae). Deutsche Entomologische Zeitschrift 61(2): 123-132. https://doi.org/10.3897/dez.61.8048
Figure 1 - Eulachnus pumilae – oviparous female: (a) general view, (b) antennal segments I–IV, (c) antennal segments V and VI, (d) apical segment of rostrum, (e) hind tibia, (f) hind tarsus with HT I parts lengths: b – basal length, d – dorsal length, v –ventral length, i – intersegmental length. Alate male: (g) head, (h) antennal segments I–IV, (i) antennal segments V and VI, (j) apical segment of rostrum, (k) hind tarsus, (l) abdomen.
Figure 3 from: Kanturski M, Wieczorek K (2014) Systematic position of Eulachnus cembrae Börner with description of hitherto unknown sexual morphs of E. pumilae Inouye (Hemiptera, Aphididae, Lachninae). Deutsche Entomologische Zeitschrift 61(2): 123-132. https://doi.org/10.3897/dez.61.8048
Figure 3 - External male genitalia of Eulachnus pumilae (a, c) and Eulachnus cembrae (b, d): bp –basal part of phallus with sclerotized arms consists of short proximal (solid arrow), long distal (dotted arrow) part and upper half-circle-shaped structure that surrounds the genital area (arrow-head), P – parameres, C – cauda.
Figure 2 from: Kanturski M, Wieczorek K (2014) Systematic position of Eulachnus cembrae Börner with description of hitherto unknown sexual morphs of E. pumilae Inouye (Hemiptera, Aphididae, Lachninae). Deutsche Entomologische Zeitschrift 61(2): 123-132. https://doi.org/10.3897/dez.61.8048
Figure 2 - Eulachnus cembrae – oviparous female: (a) general view, (b) antennal segments I–IV, (c) antennal segments V and VI, (d) apical segment of rostrum, (e) hind tibia, (f) hind tarsus. Alate male: (g) head, (h) antennal segments I–IV, (i) antennal segments V and VI, (j) apical segment of rostrum, (k) hind tarsus, (l) abdomen.
Figure 2 from: Blackman R, Nieto Nafría J, Martin J (2014) Two more new species of Aphidura (Hemiptera, Aphididae), and a note on variation in Aphidura bozhkoae Narzikulov. ZooKeys 425: 113-129. https://doi.org/10.3897/zookeys.425.7797
Figure 2 - Aphidura corsicensis sp. n., apterous viviparous female. A Habitus B Mesosternum with mammariform processes (signalled with arrows).
Figure 4 from: Blackman R, Nieto Nafría J, Martin J (2014) Two more new species of Aphidura (Hemiptera, Aphididae), and a note on variation in Aphidura bozhkoae Narzikulov. ZooKeys 425: 113-129. https://doi.org/10.3897/zookeys.425.7797
Figure 4 - Aphidura bozhkoae mesosternal processes of five apterous viviparous females collected in Ziddy (Tajikistan) in 1981 by G. Shaposhnikov, same sample as the two specimens in Figure 3.
Figure 1 from: Blackman R, Nieto Nafría J, Martin J (2014) Two more new species of Aphidura (Hemiptera, Aphididae), and a note on variation in Aphidura bozhkoae Narzikulov. ZooKeys 425: 113-129. https://doi.org/10.3897/zookeys.425.7797
Figure 1 - Aphidura libanensis sp. n., apterous viviparous females. A Habitus B Part of prothorax with a marginal tubercle (signalled with an arrow) C Marginal zone of abdominal segments 3 and 4, with marginal tubercles (signalled with arrows) D Mesosternum with mammariform processes (signalled with arrows) E Mesosternum with mammariform processes (signalled with arrows) of another specimen.
Figure 3 from: Blackman R, Nieto Nafría J, Martin J (2014) Two more new species of Aphidura (Hemiptera, Aphididae), and a note on variation in Aphidura bozhkoae Narzikulov. ZooKeys 425: 113-129. https://doi.org/10.3897/zookeys.425.7797
Figure 3 - Aphidura bozhkoae apterous viviparous females from Ziddy (Tajikistan). A–C habitus, anterior part D–E Mesosternum with mammariform processes. A specimen collected in 1954 by Narzikulov B–E Two specimens collected in 1981 by Shaposhnikov. Note the different dorsal pattern and the different size and form of processes.
Figirue 2 from: Lee W, Kanbe T, Akimoto S (2014) A new species of Megoura (Hemiptera, Aphididae) from Japan. ZooKeys 417: 37-44. https://doi.org/10.3897/zookeys.417.7167
Figirue 2 - Photographs of Megoura lathyricola sp. n. and host plant: A apterous viviparous female B alate viviparous female C Lathyrus japonicus subsp. japonicus.
Figure 1 from: Lee W, Kanbe T, Akimoto S (2014) A new species of Megoura (Hemiptera, Aphididae) from Japan. ZooKeys 417: 37-44. https://doi.org/10.3897/zookeys.417.7167
Figure 1 - Apterous viviparous female (A–H) and Alate viviparous female (I–P) of Megoura lathyricola sp. n.: A whole body of apterous vivipara B siphunculus C hind tibia and tarsus D antennal segments III–IV E antennal segments V–VI F head focused on dorsum G ultimate rostral segment H cauda I whole body of alate vivipara J siphunculus K hind tibia and tarsus L antennal segments III–IV M antennal segments V–VI N head focused on dorsum O ultimate rostral segment P cauda.
Figure 7 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 7 - Body of alate viviparae. A Aphid glycines B Aphid gossypii C Aphid gossypii D Aphid sedi E Aphid monardae F Aphid nasturtii G Aphid oestlundi.
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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OpenNeuro
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