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Figure 2 in Size-dependent sex allocation in Solanum lycocarpum St. Hil. (Solanaceae)
Figure 2. Number of flowers per plant as a function of the plant size. The number of flowers in smaller group (minimum = 0.000; maximum = 36.00; mean = 5; median = 10.6; standard error = 2.54) versus in larger group (minimum = 3.00; maximum = 54.00; mean = 29.00; median = 30.00; standard error = 3.51).
Figure 4 in Size-dependent sex allocation in Solanum lycocarpum St. Hil. (Solanaceae)
Figure 4. Interaction between the floral attributes according to the flowers gender. The circles represent hermaphrodite flowers and the squares represent male flowers. (A) Corolla diameter (cm) versus anther size (cm); (B) Flower Biomass versus anther size (cm).
Figure 1 in Size-dependent sex allocation in Solanum lycocarpum St. Hil. (Solanaceae)
Figure 1. Flowers of Solanum lycocarpum. (A) Hermaphrodite flower; (B) Male flowers. The scale bars units were 3 cm for each picture.
Figure 2 in Sex-related differences in the postmolt distribution of Weddell seals (Leptonychotes weddellii) in the southern Weddell Sea
Figure 2. Weddell seal tracks created by interpolating estimated dive positions in time. Coastline and contours from Arndt et al. (2013) and bathymetry from ETOPO1 1 Arc-Minute Global Relief Model (Amante and Eakins 2009). Projection: Polar Stereographic. Datum: World Geodetic 1984 (WGS84).
Figure 5 in Sex-related differences in the postmolt distribution of Weddell seals (Leptonychotes weddellii) in the southern Weddell Sea
Figure 5. Resident time (the proportion of dives allocated a resident behavioral state from the state-space model taken from Bestley et al. 2015) for five male and eight female Weddell seals in region A (shallow water in the shelf), region B (deep water Filchner Trough), region C (continental shelf edge), and region D (deep water off the shelf).
Figure 1b in Sex-related differences in the postmolt distribution of Weddell seals (Leptonychotes weddellii) in the southern Weddell Sea
Figure 1b. Four regions categorized by chart contours and bathymetry. Region A is south of 74°200S and <600 m, region B is south of 74°200S and ≥600 m, region C is north of 74°400S and <2,000 m and region D is north of 74°400S and ≥2,000 m. Coastline and contours from Arndt et al. (2013) and bathymetry from ETOPO1 1 Arc-Minute Global Relief Model (Amante and Eakins 2009). Projection: Polar Stereographic. Datum: World Geodetic 1984 (WGS84).
Figure 1a in Sex-related differences in the postmolt distribution of Weddell seals (Leptonychotes weddellii) in the southern Weddell Sea
Figure 1a. Study area showing postmolt range of Weddell seals tagged with CTD-SRDLs during 2011 deployment. Axes include data on both latitude and longitude. Minimum ice extent data from January 2011 and maximum ice extent data from June 2011 (Fetterer et al. 2002). Coastline and contours from Arnt et al. (2013) and bathymetry from ETOPO1 1 Arc-Minute Global Relief Model (Amante and Eakins 2009). Projection: Polar Stereographic. Datum: World Geodetic 1984 (WGS84).
Figure 4 in Sex-related differences in the postmolt distribution of Weddell seals (Leptonychotes weddellii) in the southern Weddell Sea
Figure 4. Bathymetry in meters associated with each estimated dive position for 9 males and 10 females. Bathymetry data were extracted from ETOPO1 1 Arc-Minute Global Relief Model (Amante and Eakins 2009).
Fig. 3 in Effects of male age and mating status on response to the female sex pheromone of Copitarsia decolora (Lepidoptera: Noctuidae)
Fig. 3. Activation latencies (black bars) and landing latencies (gray bars) (Q1 <Median <Q2) of virgin and mated Copitarsia decolora males to female sex pheromone extract (3FE) in wind tunnel bioassays. Mated males were tested 24 h and 48 h afer mating (24 AM and 48 AM, respectively). Bars within a behavior headed by the same letter are not significantly different (Tukey's mean separation test, n = 10, P <0.05).
Fig. 2 in Evaluation of field dispersal and survival capacity of the genetic sexing strain Tapachula-7 of Anastrepha ludens (Diptera: Tephritidae)
Fig. 2. General displacement of Anastrepha ludens SMR strain (solid line) and Tap-7 strain (broken line) in a Cartesian plane.
Fig. 1 in Effects of male age and mating status on response to the female sex pheromone of Copitarsia decolora (Lepidoptera: Noctuidae)
Fig. 1. Activation latencies (black bars) and landing latencies (gray bars) (Q1 <Median <Q2) by age group of virgin males in response to a glandular extract of female sex pheromone (3FE) in wind tunnel bioassays. Bars within a behavior headed by the same letter are not significantly different (Tukey's mean separation test, n = 10, P <0.05).
Fig. 1 in Evaluation of field dispersal and survival capacity of the genetic sexing strain Tapachula-7 of Anastrepha ludens (Diptera: Tephritidae)
Fig. 1. Contours of displacement of the SMR strain (lef) and Tap-7 strain (right) of Anastrepha ludens inside the field plot. The density of the flies at each contour is indicated by the number.
Fig. 4 in Effects of male age and mating status on response to the female sex pheromone of Copitarsia decolora (Lepidoptera: Noctuidae)
Fig. 4. Depolarization (mean ± SEM) of antennae in response to a glandular extract of female sex pheromone (3FE) of virgin and mated males. Mated males were tested 24 h and 48 h afer mating (24 AM and 48 AM, respectively). Bars headed by the same letter are not significantly different (Tukey's mean separation test, n = 6, P <0.05).
Fig. 4 in Fig. 1 in Fig. 4 in Identification of Sexually Dimorphic Genes in Pectoral Fin as Molecular Markers for Assessing the Sex of Japanese Silver Eels ().
Fig. 4. Vizcainocypria viator gen. nov. sp. nov., male (MUVHNZY0011). A: A2. B: Right prehensile palp. C: Left prehensile palp. D: Hemipenis. E: Zenker organ. Scale bars: A–E = 50 µm.
Fig. 2 in Fig. 1 in Fig. 4 in Identification of Sexually Dimorphic Genes in Pectoral Fin as Molecular Markers for Assessing the Sex of Japanese Silver Eels ().
Fig. 2. Vizcainocypria viator gen. nov. sp. nov., female (MUVHNZY0012). A: A1 (arrow pointing to apical claw on penultimate segment). B: A2. C: Md coxa. D: Md palp. E: Detail of α and β setae. F: Mxl. Scale bars: A–F = 50 µm.
Fig. 3 in Fig. 1 in Fig. 4 in Identification of Sexually Dimorphic Genes in Pectoral Fin as Molecular Markers for Assessing the Sex of Japanese Silver Eels ().
Fig. 3. Vizcainocypria viator gen. nov. sp. nov., female (MUVHNZY0012). A: T1. B: T2. C: T3. D: CR. E: Caudal attachment. Scale bars: A–E = 50 µm.
Fig. 6 in Fig. 1 in Fig. 4 in Identification of Sexually Dimorphic Genes in Pectoral Fin as Molecular Markers for Assessing the Sex of Japanese Silver Eels ().
Fig. 6. Male copulatory organs (hemipenes) of different species of Cyclocyprididae. A: Cyclocypris, B: Cypria, C: Physocypria, D: Dentocypria, E: Keysercypria, F: Brasilocypria, G: Claudecypria, H: Vizcainocypria. Redrawn from Almeida et al. (2023): F, G; Karanovic (2011): C (P. bullata), E; Hartmann (1959): H (V. granadae); Meisch (2000): A, B (C. exsculpta, C. ophtalmica), C (P. kraepelini); Savatenalinton (2017): D; Smith and Janz (2008): B (C. matzkeae), C (P. nipponica, P. biwaensis); Wouters (1984): B (C. subsalsa). Scale bars are shown when available: D. smithi = 46 µm; C. ovum, C. ophtalmica, C. subsalsa, P. nipponica, P. biwaensis, D. mesquitai, B. pea, B. alisonae, C. mesquitai, C. rochei, V. viator = 50 µm; C. matzkeae, P. bullata, K. affinis, K. deformis = 100 µm.
Fig. 1 in Fig. 1 in Fig. 4 in Identification of Sexually Dimorphic Genes in Pectoral Fin as Molecular Markers for Assessing the Sex of Japanese Silver Eels ().
Fig. 1. Vizcainocypria viator gen. nov. sp. nov., female (A, C–G, I), male (B, H). A: Mature female specimen. B: Mature male specimen. C: CpL from right side (MUVHNZY0020). D: CpF (MUVHNZY0019). E: CpD (MUVHNZY0018). F: LVi (MUVHNZY0016). G: Detail of the internal tooth (MUVHNZY0016). H: RVi (MUVHNZY0011). I: Detail of the tubercles on RV margin (MUVHNZY0017). Scale bars: A–F, H = 200 µm; G = 10 µm; I = 5 µm.
Fig. 5. Maximum likelihood tree for 28S in Fig. 1 in Fig. 4 in Identification of Sexually Dimorphic Genes in Pectoral Fin as Molecular Markers for Assessing the Sex of Japanese Silver Eels ().
Fig. 5. Maximum likelihood tree for 28S (A) and COX1 (B) genes. Red branches indicate the presence of tubercles on the RV margin.
Fig. 8. The IL-6 in Fig. 4 in Identification of Sexually Dimorphic Genes in Pectoral Fin as Molecular Markers for Assessing the Sex of Japanese Silver Eels ().
Fig. 8. The IL-6 expression levels of Japanese eel and giant mottled eel reared in different spectra. W: white light; B: blue light; G: green light; R: red light; black: dark. Different letters indicate significant differences between different spectra groups of the same eel species (p <0.05).
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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.