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Figure 8 in Spodoptera cosmioides (Lepidoptera: Noctuidae) in Brazil: spatial distribution and relationship in the S. latifascia species group
Figure 8 Maximum likelihood tree of Spodoptera cosmioides reconstructed based on sequences of the Cytochrome oxidase subunit I gene. Sequences of S. descoinsi (blue), S. evanida, and S.latifascia taken from BOLD Systems were also included.The numbers above the branches indicate bootstrap support (asterisk indicates values below 50%). Bold indicate sequences from French Guiana (blue, S. descoinsi; black, S. cosmioides).
Figure 7 in Spodoptera cosmioides (Lepidoptera: Noctuidae) in Brazil: spatial distribution and relationship in the S. latifascia species group
Figure 7 Variation in Spodoptera cosmioides wing length for populations distributed along a latitudinal gradient in Brazil. Blue and yellow colors correspond to male and female, respectively. Box plots represent medians and quartiles.
Figure 6 in Spodoptera cosmioides (Lepidoptera: Noctuidae) in Brazil: spatial distribution and relationship in the S. latifascia species group
Figure 6 Lectotype of Spodoptera cosmioides (A), paratype of S. descoinsi (B), possible (syn)type of S. latifascia (C), and lectotypeof Prodenia variolosa Walker, a junior synonym of S. latifascia (D), under dorsal view. Dorsal and ventral views of a specimen of S. evanida (E). Scale bar: 10 mm.
Figure 1 in Spodoptera cosmioides (Lepidoptera: Noctuidae) in Brazil: spatial distribution and relationship in the S. latifascia species group
Figure 1 Geographical distribution of Spodoptera cosmioides and S. latifascia from the literature (Pogue, 2002; Dumas et al., 2015), field collection, and museum records obtained in the present study.
Figure 9 Evolutionary relationships within the S in Spodoptera cosmioides (Lepidoptera: Noctuidae) in Brazil: spatial distribution and relationship in the S. latifascia species group
Figure 9 Evolutionary relationships within the S. latifascia group based on sequences of the Cytochrome oxidase subunit I gene (COI). Median-joining network among COI haplotypes (A). Haplotype frequency is indicated by the circle size (given in the inlet). Distribution of the five haplotypes identified in cosmioides+ descoinsi clade indicated by circles of fixed size, colored, according to the proportion of occurrence for each site (B).
Figure 5 in Spodoptera cosmioides (Lepidoptera: Noctuidae) in Brazil: spatial distribution and relationship in the S. latifascia species group
Figure 5 Variation in dorsal wing color pattern in Spodoptera cosmioides. A-B Rio Branco: A #m, B #f (left forewing); C-D Planaltina: C #m, D #f (left forewing); E-F Chapadão do Sul: E #m, F #f (left forewing); G-H Alegre:G #m, H #f (left forewing); I-J Londrina: I #m, J #f (left forewing); K-L Passo Fundo: K #m, L #f (left forewing). Scale bars: 5 mm, respectively.
Figure 2 in Spodoptera cosmioides (Lepidoptera: Noctuidae) in Brazil: spatial distribution and relationship in the S. latifascia species group
Figure 2 Geographical distribution of Spodoptera evanida and S. descoinsi from the literature (Pogue, 2002; Dumas et al., 2015; GBIF Secretariat, 2023).
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. Phylogram showing phylogenetic relationships estimated using maximum likelihood analysis of 16S rRNA and COXI gene revealed the grouping of Orthochirus iranus, O. farzanpay, O. stockwelli, O. zagrosensis, O. innesi (JQ514244.1 Morocco), and O. bicolor (KT716038.1 India), with the outgroup species Androctonus crassicauda (FJ217732). in A study of genetic diversity among different population of Orthochirus sp. based on cytochrome C oxidase subunit I and 16srRNA sequencing
Figure. Phylogram showing phylogenetic relationships estimated using maximum likelihood analysis of 16S rRNA and COXI gene revealed the grouping of Orthochirus iranus, O. farzanpay, O. stockwelli, O. zagrosensis, O. innesi (JQ514244.1 Morocco), and O. bicolor (KT716038.1 India), with the outgroup species Androctonus crassicauda (FJ217732).
Figure 2 in Length-weight relationships and condition factor of five endemic fish species from Nandu and Wanquan Rivers in Hainan Island, China
Figure 2. Length-length relationships of the 5 fish species collected from June 2017 to April 2019 in the Nandu and Wanquan Rivers.
Figure 1 in Length-weight relationships and condition factor of five endemic fish species from Nandu and Wanquan Rivers in Hainan Island, China
Figure 1. Length-weight relationships of the 5 fish species collected from June 2017 to April 2019 in the Nandu and Wanquan Rivers.
Figure 5 in Evolutionary relationships among several species from the genus Cricotopus (Diptera: Chironomidae): What about Turkish representatives of this genus?
Figure 5. BEAST chronogram of divergence of the representatives of the genus Cricotopus. Specimens collected and sequenced in this study are demonstrated in bold. Time to most recent common ancestor (tmrca) was estimated for the lettered nodes (in red) which correspond with those in Table 4. The time scale is in millions of years before present.
Figure 4. A neighbour-net phylogenetic network constructed using 106 in Evolutionary relationships among several species from the genus Cricotopus (Diptera: Chironomidae): What about Turkish representatives of this genus?
Figure 4. A neighbour-net phylogenetic network constructed using 106 COI sequences of the genus Cricotopus and two COI sequences Orthocladius sp. (outgroup). For the clarity of the network, bootstrap support values of the nodes are not demonstrated.
Figure 3 in Evolutionary relationships among several species from the genus Cricotopus (Diptera: Chironomidae): What about Turkish representatives of this genus?
Figure 3. Bayesian tree based on the analysis of COI sequences. Node-associated values (in red) correspond to ML bootstrap support (BS) and BI posterior probabilities (PP), respectively. Full support (100%/1.00) is marked with a bold circle.
Figure 2 in Evolutionary relationships among several species from the genus Cricotopus (Diptera: Chironomidae): What about Turkish representatives of this genus?
Figure 2. Saturation plot for transitions (blue crosses) and transversions (green triangles). The x axis shows the genetic distance based on the GTR model, while the y axis shows the proportion of transitions and transversions. The lines show the trends of the variance of transitions and transversions with increasing genetic distance.
Figure 3. The species−area relationship for 94 in The land snails of Lichadonisia islets (Greece)
Figure 3. The species−area relationship for 94 islets of the Aegean Sea, of similar size with the islets of Lichadonisia, i.e. less than 1.5 km2 and the respective position of the three islets presented with red dots.
Figure 1 in Condition factor and length-weight relationships evaluation of 15 Oxynoemacheilus species (Cypriniformes: Nemacheilidae) from Iran
Figure 1. Box plot of (a) allometric coefficient b values, (b) Fulton's condition factor (K F) for 15 Oxynoemacheilus species from Iran.
Fig. 20 in Putative relationships among inseminating and externally fertilizing characids, with a description of a new genus and species of Brazilian inseminating fish bearing an anal-fin gland in males (Characiformes: Characidae)
Fig. 20. Light micrographs through gill gland of mature male Bryconadenos tanaothoros, SL 36.6 mm (USNM 352061). A, entire gill gland showing chambers (c) containing some stained material; unmodified gills are seen at the extreme left and right; bar, 100 µm. B, Enlargement of same specimen showing one chamber (c) with tall columnar cells in between reduced secondary lamellae (arrows); bar, 20 µm.
Fig. 19. Light micrographs through gill glands.A in Putative relationships among inseminating and externally fertilizing characids, with a description of a new genus and species of Brazilian inseminating fish bearing an anal-fin gland in males (Characiformes: Characidae)
Fig. 19. Light micrographs through gill glands.A, male Attonitus bounites, SL 43.0 mm (USNM 349701), longitudinal section through gill gland showing the ventral epithelium (arrows) that results in the formation of gill gland chambers (c); arrowhead indicates an unmodified gill filament; bar, 200 µm. B, same specimen showing tall columnar cells (arrows) in between reduced secondary lamellae; s, secretory material; bar, 50 µm. C, male A. irisae, SL 46.1 mm (USNM 349698), longitudinal section through immature gill gland showing the epithelium (arrows) covering the gland chambers (c); bar, 200 µm.
Fig. 17 in Putative relationships among inseminating and externally fertilizing characids, with a description of a new genus and species of Brazilian inseminating fish bearing an anal-fin gland in males (Characiformes: Characidae)
Fig. 17. Scanning electron micrograph of spermatozoon in testis of male Bryconadenos tanaothoros (MCP 30333); arrow indicates point of exit of the flagellum from the cytoplasmic collar; bar, 1 µm.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.