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348 results for “seagrass”
FIGURE 1 in New Leptocheliidae (Crustacea: Tanaidacea: Tanaidomorpha) from Australian seagrass and macro-algal habitats, and a redescription of the poorly-known Leptochelia ignota from Sydney Harbour
FIGURE 1. Leptochelia ignota. Quarantine Bay, Sydney Harbour, NSW. Female lateral, antennule (A1), antenna (A2), cheliped (CH), pleotelson (Plt). Scale units 0.1 mm for full appendages.
FIGURE 16 in New Leptocheliidae (Crustacea: Tanaidacea: Tanaidomorpha) from Australian seagrass and macro-algal habitats, and a redescription of the poorly-known Leptochelia ignota from Sydney Harbour
FIGURE 16. Parakonarus robertsoni. Seven Mile Beach, WA. Female. Pereopods 1–6 (P1–P6), pleopod (Pl). Scale units 0.1 mm for full appendages.
FIGURE 11 in New Leptocheliidae (Crustacea: Tanaidacea: Tanaidomorpha) from Australian seagrass and macro-algal habitats, and a redescription of the poorly-known Leptochelia ignota from Sydney Harbour
FIGURE 11. Poorea wrighti. Cliff Head, WA. Male. Pereopods 1–6 (P1–P6), pleopod (Pl), uropod (U). Scale units 0.1 mm for full appendages.
FIGURE 13 in New Leptocheliidae (Crustacea: Tanaidacea: Tanaidomorpha) from Australian seagrass and macro-algal habitats, and a redescription of the poorly-known Leptochelia ignota from Sydney Harbour
FIGURE 13. Poorea johannesi. Cliff Head, WA. Male. Pereopods 1–6 (P1–P6), pleopod (Pl), uropod (U). Scale units 0.1 mm for full appendages.
FIGURE 8 in New Leptocheliidae (Crustacea: Tanaidacea: Tanaidomorpha) from Australian seagrass and macro-algal habitats, and a redescription of the poorly-known Leptochelia ignota from Sydney Harbour
FIGURE 8. Leptochelia gadgeti. Cliff Head, WA. Male dorsal (holotype), antennule (A1), antenna (A2), cheliped (CH), pleotelson (Plt). Scale units: 1 mm for whole animal, 0.1 mm for appendages.
FIGURE 7 in New Leptocheliidae (Crustacea: Tanaidacea: Tanaidomorpha) from Australian seagrass and macro-algal habitats, and a redescription of the poorly-known Leptochelia ignota from Sydney Harbour
FIGURE 7. Leptochelia evansi. Seven Mile Beach, WA. Male. Pereopods 1–6 (P1–P6), pleopod (Pl), uropod (U). Scale units 0.1 mm for full appendages.
FIGURE 4 in New Leptocheliidae (Crustacea: Tanaidacea: Tanaidomorpha) from Australian seagrass and macro-algal habitats, and a redescription of the poorly-known Leptochelia ignota from Sydney Harbour
FIGURE 4. Leptochelia ignota. Quarantine Bay, Sydney Harbour, NSW. Male dorsal (holotype), antennule (A1), antenna (A2), cheliped (CH), pleotelson (Plt). Scale units 0.1 mm for full appendages.
FIGURE 12 in New Leptocheliidae (Crustacea: Tanaidacea: Tanaidomorpha) from Australian seagrass and macro-algal habitats, and a redescription of the poorly-known Leptochelia ignota from Sydney Harbour
FIGURE 12. Poorea johannesi. Cliff Head, WA. Male dorsal (holotype), antennule (A1), antenna (A2), cheliped (CH), pleotelson (Plt). Scale units 0.1 mm for full appendages.
FIGURE 5 in Two new species of the genus Daptonema Cobb, 1920 (Nematoda: Xyalidae) found in the monospecific Halophila ovalis patches within an intertidal mixed-species seagrass bed on the coast of the Andaman Sea, Thailand
FIGURE 5. Daptonema setihyalocella sp. n. Male (Holotype ZIHU 4081): A) Epidermal cells showing transparent appearance of the ventral chord in the anterior region. B) Epidermal cells showing transparent appearance of the dorsal chord in the anterior region. C) Amphid and epidermal cells showing transparent appearance of the lateral chord in the head region. D) Spicule and gubernaculum. Female (Allotype ZIHU 4085): E) Eggs and sperm cells in the uterus. F) Flat vulval gland. D, computer-integrated composite of original photomicrographs. A–E, left side view; F, right side view. Bar scales: A, B, 20 µm; C, D, F, 10 µm; E, 50 µm. Abbreviations: asterisk (*)—epidermal cell showing transparent appearance, amp—amphid, da —dorsal apophysis of gubernaculum, e—egg, gub —gubernaculum, lp—lateral piece of gubernaculum, ph—pharynx, s —sperm cell, spic —spicule, u —uterus, v —vulva, vgl —flat vulval gland.
FIGURE 2 in Two new species of the genus Daptonema Cobb, 1920 (Nematoda: Xyalidae) found in the monospecific Halophila ovalis patches within an intertidal mixed-species seagrass bed on the coast of the Andaman Sea, Thailand
FIGURE 2. Daptonema hyalocella sp. n. Male (Holotype ZIHU 3811; left side view): A) Entire body. B) Anterior region. C) Head region. D) Posterior region. E) Spicules and gubernaculum. Female (Allotype ZIHU 3817; left side view): F) Entire body. G) Vulval region. H) Posterior region. Bar scales: A, F, 100 µm; B, D, G, H: 20 µm; C, E, 10µm.
FIGURE 1 in Two new species of the genus Daptonema Cobb, 1920 (Nematoda: Xyalidae) found in the monospecific Halophila ovalis patches within an intertidal mixed-species seagrass bed on the coast of the Andaman Sea, Thailand
FIGURE 1. Location of the study site in the seagrass bed near Ban Pa Khlok, Phuket Province, Thailand. Asterisk, study site (8º 01' 20'' N, 98º 24' 40'' E).
FIGURE 3 in Two new species of the genus Daptonema Cobb, 1920 (Nematoda: Xyalidae) found in the monospecific Halophila ovalis patches within an intertidal mixed-species seagrass bed on the coast of the Andaman Sea, Thailand
FIGURE 3. Daptonema hyalocella sp. n. Male (A–C, Holotype ZIHU 3811; D, additional specimen): A) Epidermal cells showing transparent appearance of the dorsal and ventral chords in the head region. B) Amphid and epidermal cells showing transparent appearance of the lateral chord in the anterior region. C) Distal portion of the spicule and lateral piece of the gubernaculum. D) Epidermal cells showing transparent appearance of the dorsal, lateral and ventral chords in the pharyngeal region; transverse section, top is dorsal side. Female (Allotype ZIHU 3817): E) Epidermal cells showing transparent appearance of the dorsal and ventral chords in the anterior region. F) Uterus and postvulval sac in the vulval region. A–C, E, F, left side view; D, en face view. B, C, computer-integrated composite of original photomicrographs. Bar scales: A–D, 10 µm; E, F, 20 µm. Abbreviations: asterisk (*)—epidermal cell showing transparent appearance, amp—amphid, lp—lateral piece of gubernaculum, ph —pharynx, pvs —postvulval sac, spic—spicule, u —uterus, v—vulva.
FIGURE 4 in Two new species of the genus Daptonema Cobb, 1920 (Nematoda: Xyalidae) found in the monospecific Halophila ovalis patches within an intertidal mixed-species seagrass bed on the coast of the Andaman Sea, Thailand
FIGURE 4. Daptonema setihyalocella sp. n. Male (Holotype ZIHU 4081, left side view): A) Entire body. B) Anterior region. C) Head region. D) Posterior region. E) Spicule and gubernaculum. Female (Allotype ZIHU 4085; left side view): F) Entire body. G) Vulval region. H) Posterior region. Bar scales: A, F, 100 µm; B, D, H, 40 µm; C, E, 20 µm; G, 50 µm.
FIGURE 3 in A new species of seagrass-boring Limnoria (Limnoriidae, Isopoda, Crustacea) from Japan
FIGURE 3. Limnoria rhombipunctata sp. nov. Holotype, male, KMNH IvR 500862: A, pleopod 1; B, pleopod 2; C, pleopod 3; D, pleopod 4; E, pleopod 5; G, posterior margin of pleotelson. Paratype, male, KMNH IvR 500867: F, penes; H, left uropod. Scale bars: A–E = 0.25 mm, F, H = 0.1 mm. G = 0.02 mm.
FIGURE 1 in A new species of seagrass-boring Limnoria (Limnoriidae, Isopoda, Crustacea) from Japan
FIGURE 1. Limnoria rhombipunctata sp. nov. Holotype, male, KMNH IvR 500862: A, dorsal view; B, pleotelson; C, antenna 1; D, antenna 2; E, maxilla 1; F, maxilla 2; G, maxilliped; Scale bars: A = 0.5 mm, B = 0.2 mm, C–D, G = 0.1 mm, E–F = 0.05 mm.
FIGURE 2 in A new species of seagrass-boring Limnoria (Limnoriidae, Isopoda, Crustacea) from Japan
FIGURE 2. Limnoria rhombipunctata sp. nov. Holotype, male, KMNH IvR 500862: A, left mandible; B, lacinia mobilis of right mandible; C, apical region of pereopod 1; D, pereopod 1; E, pereopod 2; F, pereopod 3; G, pereopod 4; H, pereopod 5; I, pereopod 6; J, pereopod 7. Scale bars: A, C–J = 0.1 mm, B = 0.05 mm.
Genomic comparison of two seagrass species
<p>The files correspond to result tables referenced in PhD thesis titled Genomic characterisation of seagrass species from two independent return to the sea events, University of Queensland, Australia (unpublished).</p>
Abrupt loss of soil organic carbon following disturbance in seagrass ecosystems
<h1><strong>Code for running the bifurcation diagrams and the sensitivity analysis of seagrass-soil model</strong></h1> <p> </p> <p>Contact: antoine.levilain18@gmail.com</p> <p> </p> <p>This repository contains the code used to conduct the figures of: Abrupt loss of soil organic carbon following disturbance in seagrass ecosystems. Each figure from the related study has its own folder, which includes the necessary scripts to rerun simulations, the output of those simulations, and the code to plot the results. By navigating to any figure’s folder, you can reproduce the simulations and visualise the results. The repository is organised to facilitate reproducibility and further exploration of the ecosystem model and its behavior under various scenarios.</p> <p>We performed our analysis using R version 3.6.3.</p> <p>Do not forget to add your working directory if you want to save the figures.</p> <p> </p> <h2>Sensitivity analysis (Figure 5, Figure S11, Figure S15 & Figure S16)</h2> <p>The “sensitivity” folder contains subfolders with the scripts required to run the global sensitivity analysis using the Sobol method for each scenario/case, along with the resulting outputs. In this analysis, higher numbers in folder names indicate a more deteriorated meadow, meaning it’s closer to the point of collapse. The analysis was conducted across different scenarios for different cases: “f” denotes the feedback case, while “no_f” represents the no feedback case. To recreate the figures, you can plot the pie charts for each scenario/case by running the sensitivity_plot.R script after setting the working directory to the appropriate subfolder.</p>
FIGURE 9 in Two new species of sea cucumbers (Echinodermata: Holothuroidea) from the seagrass meadow of Penang, Malaysia
FIGURE 9. Ossicles of Acaudina spinifera sp. nov. USMCRC-Echi 029. A–B. Spinose doughnut-shaped bodies from dorsal body wall; C. Spinose perforated plates from dorsal body wall; D. Spinose sub-spherical bodies from dorsal body wall; E. Spinose perforated plates from caudal region body wall; F. Spinose sub-spherical bodies from caudal region body wall; G. Rosettes from caudal region body wall; H. Rosette-like rods from caudal region body wall; I. Thick rounded rods from caudal region body wall; J. Dumbbell-shaped rod from caudal region body wall; K. Rosette in tentacle.
FIGURE 5 in Two new species of sea cucumbers (Echinodermata: Holothuroidea) from the seagrass meadow of Penang, Malaysia
FIGURE 5. Ossicles of Euthyonidiella zulfigaris sp. nov. USMCRC-Echi 010. A. Tables in dorsal body wall; B. Tables with three-pillared spires in dorsal body wall; C. Endplate in tube feet; D. Large rods in tentacle; E. Small rod in tentacle; F. Spinose rod in tentacle; G. Rosettes in tentacle; H. Tables in body wall near anus; I. Table in dorsal body wall.
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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.