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Figure 1. Pilumnus spinifer H. Milne Edwards, 1834. Zoea I in The complete larval development of the crab Pilumnus spinifer (Brachyura: Xanthoidea: Pilumnidae) reared in the laboratory
Figure 1. Pilumnus spinifer H. Milne Edwards, 1834. Zoea I: (A) carpace, lateral view; (A1) detail of the dorsal spine; (A2) detail of the posterio-ventral margin of the carapace; (B) carapace, frontal view. Zoea II: (C) carapace, lateral view. Zoea III: (D) carapace, lateral view. Scale bars: 0.2 mm.
Figure 1 in Reproductive strategies of two sympatric species of Hyalella Smith, 1874 (Amphipoda, Dogielinotidae) in laboratory conditions
Figure 1. Assortative mating, estimated as the relationship of male and female body size (head length in mm) for precopulatory mating pairs in Hyalella pleoacuta and H. castroi. HLm, head length of males; HLf, head length of females; n, number of individuals.
Figure 3 in Reproductive strategies of two sympatric species of Hyalella Smith, 1874 (Amphipoda, Dogielinotidae) in laboratory conditions
Figure 3. Regression analyses between body size of ovigerous females (head length—HL) and number of eggs in embryonic developmental stages and number of juveniles in H. castroi. F, fecundity.
Figure 2 in Reproductive strategies of two sympatric species of Hyalella Smith, 1874 (Amphipoda, Dogielinotidae) in laboratory conditions
Figure 2. Regression analyses between body size of ovigerous females (head length—HL) and number of eggs in embryonic developmental stages and number of juveniles of H. pleoacuta. F, fecundity.
Figure 6. Pandalus gracilis Stimpson, stage 5 in Larval development of Pandalus gracilis Stimpson (Crustacea: Decapoda: Pandalidae) reared in the laboratory
Figure 6. Pandalus gracilis Stimpson, stage 5. (A) Dorsal view (scale bar: ab); (B) lateral view (ab); (C) antennule (ad); (D) antenna (ad); (E) mandibles (ae); (F) maxillule (ae); (G) maxilla (ae); (H) first maxilliped (ae); (I) second maxilliped (ae); (J) third maxilliped (ad); (K–O) left pereiopods 1–5 (ac); (P–T) pleopods 1–5 (ae); (U) telson (ac). Scale bars: 2 mm.
Figure 2. Pandalus gracilis Stimpson, stage 1 in Larval development of Pandalus gracilis Stimpson (Crustacea: Decapoda: Pandalidae) reared in the laboratory
Figure 2. Pandalus gracilis Stimpson, stage 1. (A) Dorsal view (scale bar: ab); (B) lateral view (ab); (C) antennule (ad); (D) antenna (ad); (E) mandibles (ae); (F) maxillule (ae); (G) maxilla (ae); (H) first maxilliped (ae); (I) second maxilliped (ae); (J) third maxilliped (ad); (K) right pereiopod 2 (ac); (L–P) left pereiopods 1–5 (ac); (Q) telson (ac). Scale bars: 1 mm.
Figure 1 in Larval development of Pandalus gracilis Stimpson (Crustacea: Decapoda: Pandalidae) reared in the laboratory
Figure 1. Pandalus gracilis Stimpson. Survival and duration of larval stages reared under laboratory conditions of 15°C and 33.7‰.
Figure 4. Pandalus gracilis Stimpson, stage 3 in Larval development of Pandalus gracilis Stimpson (Crustacea: Decapoda: Pandalidae) reared in the laboratory
Figure 4. Pandalus gracilis Stimpson, stage 3. (A) Dorsal view (scale bar: ab); (B) lateral view (ab); (C) antennule (ad); (D) antenna (ad); (E) mandibles (ae); (F) maxillule (ae); (G) maxilla (ae); (H) first maxilliped (ae); (I) second maxilliped (ae); (J) third maxilliped (ad); (K–O) left pereiopods 1–5 (ac); (P–T) pleopods 1–5 (ae); (U) telson (ac). Scale bars: 2 mm.
Figure 5. Pandalus gracilis Stimpson, stage 4 in Larval development of Pandalus gracilis Stimpson (Crustacea: Decapoda: Pandalidae) reared in the laboratory
Figure 5. Pandalus gracilis Stimpson, stage 4. (A) Dorsal view (scale bar: ab); (B) lateral view (ab); (C) antennule (ad); (D) antenna (ad); (E) mandibles (ae); (F) maxillule (ae); (G) maxilla (ac); (H) first maxilliped (ae); (I) second maxilliped (ae); (J) third maxilliped (ad); (K–O) left pereiopods 1–5 (ac); (P–T) pleopods 1–5 (ae); (U) telson (ac). Scale bars: 2 mm.
Figure 3. Pandalus gracilis Stimpson, stage 2 in Larval development of Pandalus gracilis Stimpson (Crustacea: Decapoda: Pandalidae) reared in the laboratory
Figure 3. Pandalus gracilis Stimpson, stage 2. (A) Dorsal view (scale bar: ab); (B) lateral view (ab); (C) antennule (ac); (D) antenna (ac); (E) mandibles (ad); (F) maxillule (ad); (G) maxilla (ad); (H) first maxilliped (ad); (I) second maxilliped (ad); (J) third maxilliped (ac); (K–O) left pereiopods 1–5 (ac); (P) telson (ac). Scale bars: 1 mm.
Supporting dataset for "Influence of urban forms on -long-duration urban flooding: laboratory experiments and computational analysis"
<p>In this dataset, we provide two parts of data:</p> <p>(1) Figures in format .fig that are included in the main text and supplementary material</p> <p>(2) Experimental datasets for the five configurations, including flow depth, discharge partition, and the flow surface velocity,</p> <p>- the data is written in a .h5 file that can be read by different languages (ex. Python),</p> <p>- a document PDF and a text file are available to visualize the data structure</p> <p>- a code of Python for reading the data in the .h5 file </p> <p> </p>
Fig. 1 in The Lecithotrophic Zoea Of Chirostylus Ortmanni Miyake & Baba, 1968 (Crustacea: Anomura: Galatheoidea: Chirostylidae) Described From Laboratory Hatched Material
Fig. 1. Chirostylus ortmanni Miyake & Baba, 1968: a, anterior view of carapace; b, antennule; c, antenna.
Fig. 7 in The Lecithotrophic Zoea Of Chirostylus Ortmanni Miyake & Baba, 1968 (Crustacea: Anomura: Galatheoidea: Chirostylidae) Described From Laboratory Hatched Material
Fig. 7. Chirostylus ortmanni Miyake & Baba, 1968: A, gravid female (ZRC 2007.0701); B, whole view of first stage zoea (ZRC 2007.0701).
Fig. 6 in The Lecithotrophic Zoea Of Chirostylus Ortmanni Miyake & Baba, 1968 (Crustacea: Anomura: Galatheoidea: Chirostylidae) Described From Laboratory Hatched Material
Fig. 6. Chirostylus ortmanni Miyake & Baba, 1968: a, second pleopod; b, third pleopod; c, fourth pleopod; d, fifth pleopod; e, uropod; f, dorsal view of telson.
Fig. 4 in The Lecithotrophic Zoea Of Chirostylus Ortmanni Miyake & Baba, 1968 (Crustacea: Anomura: Galatheoidea: Chirostylidae) Described From Laboratory Hatched Material
Fig. 4. Chirostylus ortmanni Miyake & Baba, 1968: a, first (chela) pereiopod; b, second pereiopod; c, third pereiopod; d, fourth pereiopod; e, fifth pereiopod.
FIGURE 9 in Laboratory Hybridization among North American Whiptail Lizards, Including Aspidoscelis inornata arizonae × A. tigris marmorata (Squamata: Teiidae), Ancestors of Unisexual Clones in Nature
FIGURE 9. Testis, adrenal gland, mesonephros, and vas deferens of A. t. marmorata, the father of the hybrids. A. Testis, adrenal gland, mesonephros, and vas deferens (AMNH R-153156, slide 8, row 1, section 2). B. Seminiferous tubule (AMNH R-153156, slide 8, row 1, section 2). C. Vas deferens containing mature spermatozoa (AMNH R-153156, slide 9, row 1, section 6). D. Vas deferens with mature spermatozoa (AMNH R-153156, slide 6, row 1, section 2, Mallory Triple, Pantin method). Scale bar: 0.1 mm except for A, 1.0 mm.
FIGURE 5 in Laboratory Hybridization among North American Whiptail Lizards, Including Aspidoscelis inornata arizonae × A. tigris marmorata (Squamata: Teiidae), Ancestors of Unisexual Clones in Nature
FIGURE 5. Pattern of morphological variation expressed by the distribution of scores on the first two principal components extracted from a correlation matrix of seven meristic characters of three laboratory hybrids, 18 specimens of A. i. arizonae (including the maternal parent of the hybrids), and 18 specimens of A. t. marmorata (including the paternal parent of the hybrids). All samples represent populations in the vicinities of those from which the parents of the hybrids were collected. Note that the three hybrids are intermediate to their individual parents on PC1.
FIGURE 12 in Laboratory Hybridization among North American Whiptail Lizards, Including Aspidoscelis inornata arizonae × A. tigris marmorata (Squamata: Teiidae), Ancestors of Unisexual Clones in Nature
FIGURE 12. The large tissue sample from the adult-sized, apparently female (but intersex) laboratory hybrid (AMNH R-153158). A. An entire section (AMNH R-153158A, slide 1, section 3; scale bar: 1 mm). Rectangles identify enlarged views in B–E. B. Adrenal gland (AMNH R-153158A, slide 1, section 3). C and D. Adrenal gland and transition to adjacent ovary (AMNH R-153158A, slide 1, section 3). E. Ovary (AMNH R-153158A, slide 1, section 3). Scale bars for B–E: 0.1 mm.
FIGURE 1 in Laboratory Hybridization among North American Whiptail Lizards, Including Aspidoscelis inornata arizonae × A. tigris marmorata (Squamata: Teiidae), Ancestors of Unisexual Clones in Nature
FIGURE 1. Karyotype of laboratory hybrid of A. i. arizonae (♀) × A. t. marmorata (♂), AMNH R-153158, adult-sized intersex individual that superficially resembled a female. Upper row represents the haploid complement of A. t. marmorata (with 3 large Set I metacentric and submetacentric macrochromosomes including the X + 8 biarmed Set II macrochromosomes + 12 Set III microchromosomes). Lower row represents the haploid complement of A. i. arizonae (with 1 Set I macrochromosome including its characteristic NOR and satellite [arrow] + 12 subtelocentric Set II macrochromosomes + 10 Set III microchromosomes). Line represents 10 microns.
FIGURE 6 in Laboratory Hybridization among North American Whiptail Lizards, Including Aspidoscelis inornata arizonae × A. tigris marmorata (Squamata: Teiidae), Ancestors of Unisexual Clones in Nature
FIGURE 6. Pattern of morphological variation expressed by the distribution of scores on the first two principal components extracted from a correlation matrix of seven meristic characters of three hybrids, 18 specimens of A. i. arizonae (including the maternal parent of the hybrids), 18 specimens of A. t. marmorata (including the paternal parent of the hybrids), and 11 specimens of the unisexual A. neomexicana. All samples represent populations in the vicinities of those from which the parents of the hybrids were collected. Note that the three hybrids are intermediate to their individual parents and that A. neomexicana most closely resembles its maternal progenitor species, A. t. marmorata on PC1.
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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.