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972 results for “morphological barcode”
FIGURE 5 in Morphology, molecular phylogenetics, and DNA barcoding revealed a new unusual species of the aphid genus Pleotrichophorus from the USA (Insecta, Hemiptera Aphididae)
FIGURE 5. Scanning electron microscopy (SEM) of apterous viviparous female of Pleotrichophorus blackmani sp. n.: (a) dorsal habitus; (b) head and pronotum; (c) posterior part of abdomen dorsally; (d) surface of SIPH; (e) distal tip of SIPH; (f) lateral side of the end of abdomen; (g) cauda, H—head, Pr—pronotum, MS—mesonotum, Mt—metanotum, I-VIII-abd. tergites I-VIII, s—siphunculi, c—cauda, ap—anal plate, gp—genital plate.
FIGURE 9 in Morphology, molecular phylogenetics, and DNA barcoding revealed a new unusual species of the aphid genus Pleotrichophorus from the USA (Insecta, Hemiptera Aphididae)
FIGURE 9. SEM of Pleotrichophorus blackmani sp. n. apterous viviparous female. antennal sensilla: (a) small multiporous placoid sensilla (red) and type I trichoid sensilla (blue) on ANT III; (b, c) structure of small multiporous placoid sensilla with secretion; (d) ultrastructure of the sensillum membrane; (e-g) large multiporous placoid sensillum (yellow) and type I trichoid sensilla (blue) on ANT V general view; (h-i) ultrastructure of the large multiporous placoid sensillum; (j) ANT VI BASE with sensilla on the distal end; (k) large multiporous placoid sensillum (yellow); (l) small multiporous placoid sensilla (green) and sunken coeloconic sensilla (pink); (m) ultrastructure of the secretion on sensilla surface; (n) ultrastructure of large multiporous placoid sensillum; (o) ultrastructure of sunken coeloconic sensillum.
FIGURE 3 in Morphology, molecular phylogenetics, and DNA barcoding revealed a new unusual species of the aphid genus Pleotrichophorus from the USA (Insecta, Hemiptera Aphididae)
FIGURE 3. Detailed morphological characters of Pleotrichophorus blackmani sp. n. Apterous viviparous female: (a) head setae; (b) secondary rhinaria on ANT III; (c) ANT III chaetotaxy; (d) posterior part of abdomen; (e) SIPH; (f) cauda; alate viviparous female: (g) secondary rhinaria on ANT III; (h) URS; (i) fore wing.
FIGURE 7 in Morphology, molecular phylogenetics, and DNA barcoding revealed a new unusual species of the aphid genus Pleotrichophorus from the USA (Insecta, Hemiptera Aphididae)
FIGURE 7. SEM of Pleotrichophorus blackmani sp. n. apterous viviparous female, thorax and abdomen surface: (a) thorax surface with trichoid sensillum (arrow); (b) abdomen general surface structure with trichoid sensilla (arrows); (c) abdomen surface with wax layer; (d) ultrastructure of the wax secretion; (e) structure of the surface of cuticle without wax (f) ultrastructure of the surface without wax.
FIGURE 8 in Morphology, molecular phylogenetics, and DNA barcoding revealed a new unusual species of the aphid genus Pleotrichophorus from the USA (Insecta, Hemiptera Aphididae)
FIGURE 8. SEM of Pleotrichophorus blackmani sp. n. apterous viviparous female. antennal sensilla: (a) dorsal side of the pedicel with campaniform sensillum (star); (b, c) ventral side of the pedicel with rhinariolum (arrow); (d) structure of trichoid sensillum on the pedicel; (e, f) ultrastructure of the rhinariola; (g) ultrastructure campaniform sensillum; (h) type I trichoid sensilla on ANT III; (i) ultrastructure of type I trichoid sensillum; (j-l) structure and ultrastructure of type II trichoid sensilla on PT.
FIGURE 2 in Morphology, molecular phylogenetics, and DNA barcoding revealed a new unusual species of the aphid genus Pleotrichophorus from the USA (Insecta, Hemiptera Aphididae)
FIGURE 2. Habitus of slide-mounted specimens of Pleotrichophorus blackmani sp. n.: (a) apterous viviparous female; (b) alate viviparous female.
FIGURE 6 in Morphology, molecular phylogenetics, and DNA barcoding revealed a new unusual species of the aphid genus Pleotrichophorus from the USA (Insecta, Hemiptera Aphididae)
FIGURE 6. SEM of Pleotrichophorus blackmani sp. n. apterous viviparous female, head surface: (a) general view; (b) general structure of the head surface and compound eye; (c) head trichoid sensilla; (d) structure of the sensillum on frons; (e, f, g) structure of the surface of cuticle and trichoid sensilla; (h) ultrastructure od the trichoid sensillum socket and basal part with molting pore (arrow); (i) ultrastructure of the trichoid sensillum apex.
FIGURE 1 in Morphology, molecular phylogenetics, and DNA barcoding revealed a new unusual species of the aphid genus Pleotrichophorus from the USA (Insecta, Hemiptera Aphididae)
FIGURE 1. Pleotrichophorus blackmani sp. n. on Euthamia graminifolia in life: (a, b) apterous viviparous females; (c, d) alate viviparous females. Photographs by Lyle J. Buss, University of Florida.
FIGURE 1 in Additional description on morphology of the Misol snake eel from Taiwan, with four verified barcodes of life sequences
FIGURE 1. Lateral view of Yirrkala misolensis. (A) Before fixing, TOU-AE7866, 351 mm TL with broken tail, Ke-tzu-liao fish market, Kaohsiung, Taiwan. Scale represents 10 mm. The position of dorsal fin origin and vent marked with red arrows. The center is a close-up view of cephalic part (Photo by W. -C. Huang). (B) When preserved, NMMB-P12003, 486 mm TL, mature female, Dong-gang fish market, Ping-tung, Taiwan, the position of dorsal fin origin and vent marked with pins.
FIGURE 3 in Additional description on morphology of the Misol snake eel from Taiwan, with four verified barcodes of life sequences
FIGURE 3. Neighbor-joining tree based on CO1 sequences, constructed using the specimens mentioned in the present study and 1 congener from NCBI. The bar indicates the evolutionary distances which were computed using the Kimura 2-parameter method with 10,000 bootstrap-replicated.
FIGURE 2 in Additional description on morphology of the Misol snake eel from Taiwan, with four verified barcodes of life sequences
FIGURE 2. Illustration of Yirrklala misolensis, NMMB-P12003, 486 mm TL, mature female, Dong-gang fish market, Pingtung, Taiwan. (A) Lateral view of head, arrows show the position of frontal pore and supratemporal pore. (B) Dentition.
FIGURE 3 in Triplax sulphuricollis Reitter, 1887 from the Hyrcanian forests of Iran recognized as a valid species by morphology and barcoding (Coleoptera: Erotylidae)
FIGURE 3. Localities of sampled specimens of Triplax collaris (Schaller, 1783) and T. sulphuricollis Reitter, 1887 examined in this study. The Hyrcanian forest in northern Iran and Azerbaijan is depicted by a dark green line.
FIGURE 2 in Triplax sulphuricollis Reitter, 1887 from the Hyrcanian forests of Iran recognized as a valid species by morphology and barcoding (Coleoptera: Erotylidae)
FIGURE 2. (a) Dorsal view and (b) ventral view of Triplax collaris (Schaller, 1783) (Austria, Neusiedler See, 05.05.1989, leg. Dries, col H. Bussler) (c) Dorsal view of male Triplax sulphuricollis (Iran, Chalandar, 36.94225°, 51.64551°, 30.06.2014, leg. S. Thorn) with characteristic orange-yellow antennal club and linear punctation in depressed rows on elytra, (d) ventral view, (e) male genitalia and (f) female genitalia.
FIGURE 1 in Triplax sulphuricollis Reitter, 1887 from the Hyrcanian forests of Iran recognized as a valid species by morphology and barcoding (Coleoptera: Erotylidae)
FIGURE 1. Neighbor-joining tree based on COI barcodes of Triplax sulphuricollis Reitter, 1887 and its presumed sister species, Triplax collaris (Schaller, 1783), created in BOLD. Genbank accession numbers age given along with species names.
Supplementary material 6 from: Rozo-Lopez P, Mengual X (2015) Mosquito species (Diptera, Culicidae) in three ecosystems from the Colombian Andes: identification through DNA barcoding and adult morphology. ZooKeys 513: 39-64. https://doi.org/10.3897/zookeys.513.9561
NJ tree based on 1,292 sequences of Neotropical mosquitoes: Explanation note: Original Neighbour-Joining tree of the barcoding sequences of mosquito species listed for the Neotropics, based on Tamura-Nei genetic distances (.tre).
Supplementary material 2 from: Rozo-Lopez P, Mengual X (2015) Mosquito species (Diptera, Culicidae) in three ecosystems from the Colombian Andes: identification through DNA barcoding and adult morphology. ZooKeys 513: 39-64. https://doi.org/10.3897/zookeys.513.9561
COI mosquito sequences downloaded from NCBI and BOLD: Explanation note: Sequences from NCBI and BOLD. Sequences downloaded between December 2013 and February 2014 for all identified species with a minimum length of 480 bp of COI barcoding region, no stop codons and possible alignment among the majority of the sequences. Total of 1,159 sequences. In blue: Additional species sequences from other geographic areas for those Neotropical groups without available sequences from the Neotropics.
Supplementary material 8 from: Rozo-Lopez P, Mengual X (2015) Mosquito species (Diptera, Culicidae) in three ecosystems from the Colombian Andes: identification through DNA barcoding and adult morphology. ZooKeys 513: 39-64. https://doi.org/10.3897/zookeys.513.9561
ML tree based on 1,292 sequences of Neotropical mosquitoes: Explanation note: Original Maximum likelihood tree of the barcoding sequences of mosquito species listed for the Neotropics (.tre).
Supplementary material 1 from: Rozo-Lopez P, Mengual X (2015) Mosquito species (Diptera, Culicidae) in three ecosystems from the Colombian Andes: identification through DNA barcoding and adult morphology. ZooKeys 513: 39-64. https://doi.org/10.3897/zookeys.513.9561
Mosquito specimens collected in the present study: Explanation note: Full collection site details, including geo-references and environmental conditions, of the mosquito taxa identified in this study.
Supplementary material 7 from: Rozo-Lopez P, Mengual X (2015) Mosquito species (Diptera, Culicidae) in three ecosystems from the Colombian Andes: identification through DNA barcoding and adult morphology. ZooKeys 513: 39-64. https://doi.org/10.3897/zookeys.513.9561
ML tree based on 1,292 sequences of Neotropical mosquitoes: Explanation note: Original Maximum likelihood tree of the barcoding sequences of mosquito species listed for the Neotropics.
Supplementary material 4 from: Rozo-Lopez P, Mengual X (2015) Mosquito species (Diptera, Culicidae) in three ecosystems from the Colombian Andes: identification through DNA barcoding and adult morphology. ZooKeys 513: 39-64. https://doi.org/10.3897/zookeys.513.9561
Outgroup taxa used in the present study: Explanation note: Outgroup taxa used in the present study. Sequences downloaded from BOLD between December 2013 and February 2014.
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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.