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738 results for “estuaries”
FIGURE 6 in Subsphaerolaimus minor sp. n. and Micromicron cephalatum Cobb, 1920 (Nematoda) from the Yen River Estuary of Vietnam
FIGURE 6. Pseudochromadora galeata Verschelde et al., 2006. Male. A: entire body; B, C: head; D: anterior body end; E: posterior body end; F: spicular apparatus (from Verschelde et al., 2006, Fig. 3).
FIGURE 5. Micromicron cephalatum Cobb, 1920. A in Subsphaerolaimus minor sp. n. and Micromicron cephalatum Cobb, 1920 (Nematoda) from the Yen River Estuary of Vietnam
FIGURE 5. Micromicron cephalatum Cobb, 1920. A: male, entire body; B, C: male, head; D: male, anterior body end; E: male, posterior body end, F, G: male, tail, H: male, precloacal body region; I: female tail. Scale bars: A—50 µm; D, E—20 µm; B, C, F–I—10 µm.
FIGURE 4. Micromicron cephalatum Cobb, 1920. A in Subsphaerolaimus minor sp. n. and Micromicron cephalatum Cobb, 1920 (Nematoda) from the Yen River Estuary of Vietnam
FIGURE 4. Micromicron cephalatum Cobb, 1920. A: male, entire body; B: female, entire body; C: male, head; D: spicule and gubernaculum; E: male, posterior body end. Scale bars: A, B—50 µm; E—20 µm; C—15 µm; D—10 µm.
FIGURE 1 in Subsphaerolaimus minor sp. n. and Micromicron cephalatum Cobb, 1920 (Nematoda) from the Yen River Estuary of Vietnam
FIGURE 1. Subsphaerolaimus minor sp. n. Holotype male and paratype female. A: male, entire body; B: female, entire body; C: male, head; D: female, head; E: female, vulva region; F: male, specular apparatus; G: female, tale; H: male, tail. Scale bars: A, B—75 µm; E—40 µm; G, H—30 µm; C, D– 15 µm; F—10 µm.
FIGURE 2 in Subsphaerolaimus minor sp. n. and Micromicron cephalatum Cobb, 1920 (Nematoda) from the Yen River Estuary of Vietnam
FIGURE 2. Subsphaerolaimus minor sp. n. Holotype male and paratype female. A: male, entire body; B: male, anterior body end; C: male, head; D: female, head; E: vulva region; F: male, cloaca region; G: male, tail, H: female, tail. Scale bars: A—100 µm; B, E–H—20 µm; C, D—10 µm.
FIGURE 3. Synidotea laticauda Benedict, 1897 in A new record and mitochondrial identification of Synidotea laticauda Benedict, 1897 (Crustacea: Isopoda: Valvifera: Idoteidae) from the Yangtze Estuary, China
FIGURE 3. Synidotea laticauda Benedict, 1897. Female (total length, 9.7 mm). A–G, pereopods 1–7. Scale = 1mm.
FIGURE 2. Synidotea laticauda Benedict, 1897. A–C in A new record and mitochondrial identification of Synidotea laticauda Benedict, 1897 (Crustacea: Isopoda: Valvifera: Idoteidae) from the Yangtze Estuary, China
FIGURE 2. Synidotea laticauda Benedict, 1897. A–C, female (total length, 9.7 mm); D, adult male (total length, 13.4 mm). A and D, habitus in dorsal view; B, Antenna 1 flagellum; C and E, uropod. Scale = 1mm.
FIGURE 5 in A new record and mitochondrial identification of Synidotea laticauda Benedict, 1897 (Crustacea: Isopoda: Valvifera: Idoteidae) from the Yangtze Estuary, China
FIGURE 5. Phylogram showing relationships among selected species of the family Idoteidae, inferred from ML analysis of COI sequences. Numbers below branches are bootstrap values (950 replicates); only values higher than 50% are shown.
FIGURE 1. Synidotea laticauda Benedict, 1897. A in A new record and mitochondrial identification of Synidotea laticauda Benedict, 1897 (Crustacea: Isopoda: Valvifera: Idoteidae) from the Yangtze Estuary, China
FIGURE 1. Synidotea laticauda Benedict, 1897. A, female (total length, 9.7 mm); B, adult male (total length, 13.4 mm), habitus in dorsal view. Scale = 1mm.
FIGURE 4. Synidotea laticauda Benedict, 1897 in A new record and mitochondrial identification of Synidotea laticauda Benedict, 1897 (Crustacea: Isopoda: Valvifera: Idoteidae) from the Yangtze Estuary, China
FIGURE 4. Synidotea laticauda Benedict, 1897. Adult male (total length, 13.4 mm). A–G, pereopods 1–7; H, pleopod 2 and appendix masculina; I, penial plate. Scale = 1mm.
Data in support of manuscript "Tidal intrusion fronts, surface convergence, and mixing in an estuary with complex topography"
<p>North River observational data in support of manuscript "Tidal intrusion fronts, surface convergence, and mixing in an estuary with complex topography". Fieldwork in Oct - Nov 2021. CTD data and ADCP data collected during shipboard surveys at a channel constriction and a bend. CTD data and Aquadopp data collected at multiple mooring sites.</p>
Data and code used in the article "Driving Factors of TOC Concentrations in Four Different Types of Estuaries"
<p>Data and code used in the article "Driving Factors of TOC Concentrations in Four Different Types of Estuaries", specifically included water quality, meteorological, and nutrient data from 4 in situ observations for the years 2002-2008, and example code for implementing BRT using R. Data (Figures 2, 3, 4, 10) can be uploaded for review purposes. Figures 5, 6, 7, 8, and 9 represent the output results of the machine learning model. These data can help the reader to better understand and replicate our research.</p>
Dataset from Rummel et al.: "Spatially resolved salt intrusion mechanisms in a tidal estuary and the impact of channel deepening" - Part 1
<p>Model data from the numerical setup of the Weser River Estuary used in Rummel et al. (submitted to JGR:Oceans): "Spatially resolved salt intrusion mechanisms in a tidal estuary and the impact of channel deepening" - Part 1.</p> <p>The dates in the file names are connected to specific model runs and do not explain the modelled time period.</p> <p>Explanation of datasets:</p> <ul> <li>2D_elev* - 2D model output for the entire year 2016 for validation at one location each (associated station name included in file name), original topography.</li> <li>3D_stat* - 3D model output for the entire year 2016 for validation at one location each (associated station name included in file name), original topography.</li> <li>3D_cross_30_80* - 3D model output for one month of 2016 for the model domain from Weser km 30 to 80 including variables needed for the salt transport decomposition. <ul> <li>2024-05-23 - March 2016, original topography</li> <li>2024-06-07 - March 2016, dredged topography</li> <li>2024-06-06 - September 2016, original topography (different temporal resolution)</li> <li>2024-06-10 - September 2016, dredged topography</li> </ul> </li> <li>3D_channel* - 3D model output for the navigational channel in the entire model domain for the entire year 2016. <ul> <li>2024-04-02 - original topography</li> <li>2024-05-16 - dredged topography</li> </ul> </li> <li>3D_cross_55/65_2024-09-02* - 3D model output for September 2016, original topography for crosssections at Weser km 55 and 65 including variables needed for the salt transport decomposition.</li> </ul>
Dataset from Rummel et al.: "Spatially resolved salt intrusion mechanisms in a tidal estuary and the impact of channel deepening" - Part 2
<p>Model data from the numerical setup of the Weser River Estuary used in Rummel et al. (submitted to JGR: Oceans): "Spatially resolved salt intrusion mechanisms in a tidal estuary and the impact of channel deepening" - Part 2.</p> <p>The dates in the file names are connected to specific model runs and do not explain the modelled time period.</p> <p>This dataset contains daily averaged 3D model output for the entire year 2016 of the whole model domain with the original, not dredged topography.</p> <p> </p>
Dataset from Rummel et al.: "Spatially resolved salt intrusion mechanisms in a tidal estuary and the impact of channel deepening" - Part 3
<p>Model data from the numerical setup of the Weser River Estuary used in Rummel et al. (submitted to JGR: Oceans): "Spatially resolved salt intrusion mechanisms in a tidal estuary and the impact of channel deepening" - Part 3.</p> <p>The dates in the file names are connected to specific model runs and do not explain the modelled time period.</p> <p>This dataset contains daily averaged 3D model output for the entire year 2016 of the whole model domain with the dredged topography.</p>
Figure 24 in Nereidid polychaetes (Annelida) inhabiting the inside of decaying fronds of the mangrove palm Nypa fruticans in a tropical estuary in Malaysia, with special reference to the life history of the dominant species, Namalycastis sp.
Figure 24. Seasonal change in average salinity and temperature at six sites in Setiu Wetlands, Terengganu, in Malaysia (a), rainfall amount recorded at Bukit Berangan, Setiu, based on data from CHIRPS (Funk et al. 2019) (b), during the sampling period from September 2015 to September 2016.
Figure 21 in Nereidid polychaetes (Annelida) inhabiting the inside of decaying fronds of the mangrove palm Nypa fruticans in a tropical estuary in Malaysia, with special reference to the life history of the dominant species, Namalycastis sp.
Figure 21. Seasonal change in size–frequency histogram of mean diameters of coelomic oocytes of Namalycastis sp. collected from six sites in Setiu Wetlands, Terengganu in Malaysia via seven samplings in the period from September 2015 to September 2016. n: number of females examined.
Figure 19 in Nereidid polychaetes (Annelida) inhabiting the inside of decaying fronds of the mangrove palm Nypa fruticans in a tropical estuary in Malaysia, with special reference to the life history of the dominant species, Namalycastis sp.
Figure 19. Seasonal change in mean body width of females, males, and individuals with sex unknown in pooled samples of Namalycastis sp. collected from six sites in Setiu Wetlands, Terengganu, in Malaysia via seven samplings in the period from September 2015 to September 2016.
Figure 16 in Nereidid polychaetes (Annelida) inhabiting the inside of decaying fronds of the mangrove palm Nypa fruticans in a tropical estuary in Malaysia, with special reference to the life history of the dominant species, Namalycastis sp.
Figure 16. Relationship between body width and body length of 277 complete specimens of Namalycastis sp. collected from September 2015 to September 2016 at six sites in Setiu Wetlands, Terengganu in Malaysia (Table 1).
Figure 7 in Nereidid polychaetes (Annelida) inhabiting the inside of decaying fronds of the mangrove palm Nypa fruticans in a tropical estuary in Malaysia, with special reference to the life history of the dominant species, Namalycastis sp.
Figure 7. Namalycastis sp., NSMT-Pol 113582 (4.2 mm BW, 200 mm BL) collected at Station 4 on 27 November 2015 (a, e, g); NSMT-Pol 113583 (2.5 mm BW, 250 mm BL) collected at Station 3 on 27 November 2015 (b–d); and UMT-Ann 1816 (2.6 mm BW, incomplete) collected from Station 2 on 27 November 2015 (f). (a) Sesquigomph spiniger in upper neurochaetae in posterior body. (b) Heterogomph spiniger with finely serrated blade in lower neurochaetae, chaetiger 5. (c) Heterogomph spinigers having blade with coarse serrations proximally in posterior body. (d) Heterogomph falciger with finely serrated blade, chaetiger 5. (e) Heterogomph falciger with finely serrated blade in posterior body. (f) Heterogomph falcigers having blade with coarse serrations proximally, chaetiger 200. (g) Heterogomph falcigers with finely serrated blade (f), and additional thin sesquigomph spinigers (epitokal chaetae) (ep) located at bottom position of lower neurochaetae in posterior body. Scale bars: a–e, g = 0.1 mm; f = 0.01 mm.
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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)
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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.