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4,144 results for “ITS barcode”
Figure 3 in Larva, pupa and DNA barcodes of the Neotropical geometrid moth Glena mielkei (Lepidoptera: Geometridae: Ennominae: Boarmiini)
Figure 3. Cephalic appendages of the last instar larva of G. mielkei. (A) Antenna. Scale bar = 0.1 mm. (B) External view of the labrum. (C) Internal view (epipharynx) of the labrum. Scale bar = 0.1 mm. (D) Left mandible—mesial view. Scale bar = 0.05 mm. (E) Left maxilla in ventral view. Scale bar = 0.05 mm. (F) Labium—ventral view. Scale bar = 0.05 mm.
Figure 2 in Larva, pupa and DNA barcodes of the Neotropical geometrid moth Glena mielkei (Lepidoptera: Geometridae: Ennominae: Boarmiini)
Figure 2. Chaetotaxy of the last instar larva of G. mielkei. (A) Head—frontal view. Scale bar = 0.5 mm. (B) Head—lateral view. Scale bar = 0.5 mm. (C) Thorax and anterior segments of the abdomen; circle on A2 indicates the tuberiform dorsolateral projections. (D) Posterior segments of the abdomen. (E) Prothoracic leg. Scale bar = 0.3 mm.
Figure 3 in Endogean beetles (Coleoptera) of illustrated DNA barcode library Guatemala: deep soil sampling and
Figure 3. Neighbour Joining DNA barcode tree of 75 endogean beetles from Guatemala. Terminal names consist of the most detailed current taxonomic identification (genus, tribe, or subfamily), followed by specimen number, family name, sample number, length of the DNA barcode fragment [with the number of ambiguously read bases in square brackets], BIN number, and GenBank accession number.
Figure 2 in Endogean beetles (Coleoptera) of illustrated DNA barcode library Guatemala: deep soil sampling and
Figure 2. Sampling methods of the deep soil Guatemala beetles. (A–C) pits producing samples GT12, GT16, and GT25, respectively (note that sample GT16 is from an extremely dry habitat, while sample GT25 is twice as large in volume); (D) a floating soil sample in a barrel with water; (E) scooping floating organic foam containing live beetles on a fine mesh; (F) wet samples prior to specimen extraction; (G) two aluminium thermoeclectors of the novel larger and lighter design; (H) thermoeclectors exposed to the Sun.
Figure 2 in DNA barcoding of freshwater fish from different drainage systems of Telangana in Southern India
Figure 2. Neighbour-joining phylogeny of the studied fish species depicting distinctive species clades corresponding to the morphospecies. Scale bar corresponds to the length of clade from each node.
Figure 1 in DNA barcoding of freshwater fish from different drainage systems of Telangana in Southern India
Figure 1. Map of the study area depicting the drainage systems marked by blue line, and the sampling locations marked by orange triangle shape.
Fig. 2 in First record of the sedge feeder Bactra verutana Zeller (Lepidoptera: Tortricidae) in Chile based on morphology and DNA barcodes
Fig. 2. Bayesian tree of Bactra verutana and congenerics based on sequences of the DNA barcode fragment (658 bp) of the cytochrome c oxidase subunit I (COI) gene. Node supports (posterior probability) indicated above branches.
Fig. 1 in First record of the sedge feeder Bactra verutana Zeller (Lepidoptera: Tortricidae) in Chile based on morphology and DNA barcodes
Fig. 1. Adult Bactra verutana collected in the Azapa Valley, northern Chile. (A) Male in dorsal view. (B) Female genitalia in ventral view. (C) Male genitalia in ventral view. Scale bars 1, 0.2 and 2.2 mm, respectively.
Figure 1. A neighbour-joining tree using 604 cytochrome C oxidase sub-unit I in Phylogenetic relationship among slender loris species (Primates, Lorisidae: Loris) in Sri Lanka based on mtDNA CO1 barcoding
Figure 1. A neighbour-joining tree using 604 cytochrome C oxidase sub-unit I (CO1) sequences from 7 different slender loris (Loris) taxas, rooted using slow loris (Nycticebus) sequences deposited in the GenBank.
Figure 5. A minimum evolution 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 5. A minimum evolution tree using cytochrome c oxidase subunit 1 sequences from Myzus cerasi populations.
Figure 2 in DNA barcoding of black cherry aphid Myzus cerasi (Fabricus, 1775) (Hemiptera: Aphididae) populations collected from Prunus avium and Prunus cerasus
Figure 2. Sampling locations of Myzus cerasi in different geographical regions of Turkey (Google Earth).
Figure 4. A maximum likelihood 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 4. A maximum likelihood tree using cytochrome c oxidase subunit 1 sequences from Myzus cerasi populations.
Figure 5 in Biodiversity, DNA barcoding data and ecological traits of caddisflies (Insecta, Trichoptera) in the catchment area of the Mediterranean karst River Cetina (Croatia)
Figure 5. Maximum likelihood phylogram based on a fragment of COI (DNA barcode region) showing the related relationships of the genus Glossosoma. The bootstrap values (BS) are marked on the branches in the order NJ/ML. BS values less than 80 are not shown. The groups delineated by ABGD approach are shown on the right side of the tree. Specimens which genomic DNA was extracted in this study are written in bold letter.
Figure 1 in Biodiversity, DNA barcoding data and ecological traits of caddisflies (Insecta, Trichoptera) in the catchment area of the Mediterranean karst River Cetina (Croatia)
Figure 1. Map of the study area with sampling stations. Names and corresponding abbreviations of the stations are listed in Table 1.
Figure 3 in Biodiversity, DNA barcoding data and ecological traits of caddisflies (Insecta, Trichoptera) in the catchment area of the Mediterranean karst River Cetina (Croatia)
Figure 3. MDS analysis of caddisfly fauna similarity at stations on the Cetina, the Ruda, the Grab and the Rumin rivers.
Figure 2 in Biodiversity, DNA barcoding data and ecological traits of caddisflies (Insecta, Trichoptera) in the catchment area of the Mediterranean karst River Cetina (Croatia)
Figure 2. Cluster analysis of caddisfly fauna similarity at stations on the rivers Cetina, Ruda, Grab and Rumin.
Figure 4 in First DNA barcoding of a new alien species Glycaspis brimblecombei Moore, 1964 (Hemiptera: Aphalaridae) in Croatia with a distribution note
Figure 4. Neighbor-joining phylogenetic tree constructed by sequences of the mtCOI-3P of Glycaspis brimblecombei Lokrum, Croatia of Glycaspis species from BOLD and GenBank databases, based on Kimura-2-parameter distance model. Numbers at nodes are NJ bootstrap support values calculated from 2000 bootstrap replicates.
Figure 1 in First DNA barcoding of a new alien species Glycaspis brimblecombei Moore, 1964 (Hemiptera: Aphalaridae) in Croatia with a distribution note
Figure 1. Distribution of species Glycaspis brimblecombei. A. Spread of the species G. brimblecombei. The coloration of the lines shows the spread of the species in the temporal scale (excluding localities for which the year of occurrence of the species is not known), B. and C. Location of sampling – Botanical Garden of the Institute for Marine and Coastal Research on the island of Lokrum.
Figure 3 in First DNA barcoding of a new alien species Glycaspis brimblecombei Moore, 1964 (Hemiptera: Aphalaridae) in Croatia with a distribution note
Figure 3. Developmental stages of Glycaspis brimblecombei: A. lerps, nymphs and egg cluster, B. adult (scale: 1 mm).
Figure 4 in DNA barcoding and a new taxonomic status of the Triaenodes ochreellus lefkas Malicky, 1974 (Insecta, Trichoptera) with new distribution data
Figure 4. Distribution of Triaenodes ochreellus ochreellus (green field) and Triaenodes ochreellus lefkas (blue field) with new data in Albania, Croatia and Montenegro (red points).
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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