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104 results for “heterotrophs”
Figs. A-D in Three newly recorded heterotrophic euglenids (Protist), Entosiphon oblongum, Euglena longa and Keelungia pulex from South Korea
Figs. A-D: Entosiphon oblongum (KF030). A: General appearance of cell 1, showing ventral view. B: Dorsal view of cell 1. C: Ventral view of cell 2. D: Dorsal view of cell 3; Arrowheads show grooves. E-G: Euglena longa (KF072). E: General appearance of cell 1. F: Cell 2, showing CV. G: Cell 3 showing FR. Arrow heads show paramylum granules. H-J: Keelungia pulex (KM080). H: Cell 1 and cell 2. I: General appearance of gliding cell 3. J: Cell 4 showing dorsal view and ridge (arrow head). FS: feeding siphon, AF: anterior flagellum, PF: posterior flagellum, FR: flagellar reservoir, F: flagellum, CV: contractile vacuole, IA: ingestion apparatus. All micrographs are DIC (differential interference contrast) images. Scale bar: 10 μm in (J).
Fig. 3 in First records of nine free-living heterotrophic flagellates from South Korea
Fig. 3. (a)-(f) Paracercomonas astra, showing general appearance, contractile vacuole (CV) and cytoplasmic strand (arrowheads). (a) cell 1, (b) cell 2, (c)-(f) cell 3. (g)-(i) Paracercomonas minima, (g) cell 1 showing CV, (h) cell 2, (i) cysts. (j)-(o) Paracercomonas producta, showing general appearance, contractile vacuole and cytoplasmic strand (arrowheads). (j) three different cells, (k) cell 1, (l) cell 2, (m) cell 3, (n), (o) cell 4. AF: anterior flagellum, PF: posterior flagellum. All micrographs are DIC images. Scale bar = 5 μm for all figures.
Fig. 2 in First records of nine free-living heterotrophic flagellates from South Korea
Fig. 2. (a)-(d) Cercomonas hiberna. (a) cell 1 showing contractile vacuole, (b), (c) cell 2 showing general appearance and contractile vacuole, (d) several cells showing cytoplasmic strand (St) and pseudopodia (arrowheads). (e)-(i) Cercomonas pellucida, showing general appearance, contractile vacuole (CV), cytoplasmic strand and nucleus (N) closely connected to the basal body. (e) cell 1, (f) cell 2, (g) cell 3, (h) cell 4, (i) cell 5 & 6. (j)-(o) Eocercomonas echina, showing general appearance, contractile vacuole and cytoplasmic strand. (j) cell 1, (k) cell 2, (l), (m) cell 3, (n) cell 4, (o) cell 5. AF: anterior flagellum, PF: posterior flagellum. All micrographs are DIC images with the excep- tions of (h), (i) which are phase contrast images. Scale bar in (d) = 10 μm for (d), and in (o) = 5 μm for other figures.
Fig. 1 in First records of nine free-living heterotrophic flagellates from South Korea
Fig. 1. (a)-(f) Notosolenus hemicircularis. (a), (b) cell 1 showing general appearance, (a) note the hyaline semicircular collar (arrowhead), (b) dorsal view showing dorsal ridges, (c)-(e) cell 2 showing a short anterior neck (arrowheads) and dorsal ridges (d), (f) dividing cell. (g)- (l) Thecamonas trahens, showing general appearance, nucleus (N), sleeve (arrowheads) and cytoplasmic strand (St), and note the anterior flagellum (AF). (g) cell 1, (h) cell 2, (i)-(l) cell 3. (m)-(r) Bodomorpha minima, showing general appearance and a rostrum (arrowheads). (m) cell 1, (n) cell 2, (o) cell 3, (p)-(r) cell 4. AF: anterior flagellum, PF: posterior flagellum, FR: flagellar reservoir. All micrographs are DIC images. Scale bar = 5 μm for all figures.
Fig. 4 in Characterizations of five heterotrophic nanoflagellates newly recorded in Korea
Fig. 4. (A, B) General light micrographs and sketch of Ancyromonas micra strain IG005. AF: anterior flagellum, PF: posterior flagellum, scale bar = 5 μm. Arrowhead and double arrowhead represent a shallow groove and rostrum, respectively. All micrographs are differential interference contrast (DIC) images. (C) Maximum likelihood phylogenetic tree inferred from the 18S rDNA sequences of Ancyromonadida (order) species including Ancyromonas micra strain IG005 and outgroup (Diacronema vlkiauum strain AC67 and Prymnesium patelliferum). Bootstrap support values (>70%) are shown at the nodes. Solid circles indicate a Bayesian posterior probability of 1 (posterior probability <0.75 not shown).
Fig. 3 in Characterizations of five heterotrophic nanoflagellates newly recorded in Korea
Fig. 3. (A, B) General light micrographs and sketch of Neobodo curvifilus (formerly Procryptobia sorokini) strain KM017. AF: anterior flagellum, PF: posterior flagellum, GR: granules, scale bar = 5 μm. All micrographs are differential interference contrast (DIC) images. (C) Maximum likelihood phylogenetic tree inferred from the 18S rDNA sequences of Neobodonida (order) species including Neobodo curvifilus strain KM017 and outgroup (Bodo saltans and Bodo uncinatus). Bootstrap support values (>80%) are shown at the nodes. Solid circles indicate a Bayesian posterior probability of 1 (posterior probability<0.95 not shown).
Fig. 2 in Characterizations of five heterotrophic nanoflagellates newly recorded in Korea
Fig. 2. (A, B) General light micrographs and sketch of Aplanochytrium minuta (formerly Labyrinthuloides minuta) strain PH004. AF: anterior flagellum, PF: posterior flagellum, scale bar = 5 μm. All micrographs are differential interference contrast (DIC) images. (C) Maximum likelihood phylogenetic tree inferred from the 18S rDNA sequences of Labyrinthulomycetes (class) species including Aplanochytrium minuta strain PH004 and outgroup (Wobblia lunata and Placidia cafeteriopsis). Bootstrap support values (>80%) are shown at the nodes. Solid circles indicate a Bayesian posterior probability of 1 (posterior probability<0.95 not shown).
Fig. 1 in Characterizations of five heterotrophic nanoflagellates newly recorded in Korea
Fig. 1. (A, B) General light micrographs and sketch of Cafeteria burkhardae strain PH003. AF: anterior flagellum, PF: posterior flagellum, CV: contractile vacuole, FV: food vacuole, scale bar = 5 μm. Arrowhead represents curved channel. All micrographs are differential interference contrast (DIC) images. (C, D) General light micrographs and sketch of Cafeteria graefeae strain UL001. (E) Maximum likelihood phylogenetic tree inferred from the 18S rDNA sequences of Cafeteria (genus) species including Cafeteria graefeae strain UL001 and Cafeteria burkhardae strain PH003 and outgroup (Paramonas globosa strain ATCC 50531 and Nerada mexicana strain ATCC 50535). Bootstrap support values (>70%) are shown at the nodes. Solid circles indicate a Bayesian posterior probability of 1 (posterior probability<0.95 not shown).
Fig. 1 in The Robin, Erithacus Rubecula (Passeriformes, Turdidae), As A Component Of Heterotrophic Consortia Of Forest Cenoses, Northeast Ukraine. Part 2
Fig. 1. Taxonomic diversity of the robin nidicolous fauna in different areas (A — main groups of invertebrates; B — main orders of insects).
Fig. 2. a in Free-living Heterotrophic Flagellates from Intertidal Sediments of Saros Bay, Aegean Sea (Turkey)
Fig. 2. a – Actinomonas mirabilis/Pteridomonas danica; b – Amastigomonas mutabilis; c – Ancyromonas micra; d – Bicosoeca conica; e – Caecitellus parvulus, note the mouth on the left-hand side; f – Bordnamonas tropicana; g – Cafeteria roenbergensis; h – Cyranomonas australis; i – Developayella elegans; j – Discocelis saleuta; k – Goniomonas amphinema; l – Cafeteria minuta, feeding cell; m – Anisonema acinus, dorsal view, note the ingestion organelle; n – Dinema platysomum, ventral view showing surface striations; o – Goniomonas pacifica; p – Heteronema exaratum, ventral view, general appearance of cell; q – Kathablepharis remigera; r – Massisteria marina; s – Neobodo saliens; t – Neobodo designis; u–v – Heteronema ovale, same cell; u – general appearance; v – extended cell. All micrographs are DIC images. Scale bar: 5 μm for all figures.
Fig. 3. a in Free-living Heterotrophic Flagellates from Intertidal Sediments of Saros Bay, Aegean Sea (Turkey)
Fig. 3. a – Petalomonas marginalis; b – Petalomonas minuta; c – Petalomonas ornata; d – Petalomonas poosilla; e–f – Ploeotia corrugata; e – general appearance of the cell from ventral and (f) dorsal view showing the ridges; g – Sphenomonas angusta; h – Ploeotia vitrea; i – Polyoeca dichotoma; j – Protaspis obliqua; k – Protaspis tegere; l – Salpingoeca marina; m – Pseudophyllomitus granulatus; n–p – 'Aegoni', n – postero-lateral view of the cell showing the beak – like structure; o – posterior view of the cell showing the flagellar insertions; p – general view of the cell. Scale bar: 5 μm for all figures.
Fig. 1. a in Free-living Heterotrophic Flagellates from Intertidal Sediments of Saros Bay, Aegean Sea (Turkey)
Fig. 1. a – Actinomonas mirabilis/Pteridomonas danica; b – Amastigomonas mutabilis; c – Ancyromonas micra; d – Bicosoeca conica; e – Bordnamonas tropicana; f – Caecitellus parvulus; g – Cafeteria minuta; h – Cafeteria roenbergensis; i – Cyranomonas australis; j – Developayella elegans; k – Discocelis saleuta; l – Goniomonas amphinema; m – Goniomonas pasifica; n – Kiitoksia ystava; o – Dinema platysomum; p – Anisonema acinus; q – Heteronema exaratum; r – Heteronema ovale; s – Kathablepharis remigera; t – Notosolenus canellatus; u – Massisteria marina; v – Metromonas grandis; w – Neobodo designis; x – Neobodo saliens; y – Percolomonas similis. Scale bar: 10 μm for all figures.
Fig. 1 in Heterotrophic Flagellates from Freshwater and Soil Habitats in Subtropical China (Wuhan Area, Hubei Province)
Fig. 1. Location of studied sites. 1 – Yangtze River, 2 – Moshan hill, 3 – Donghu Lake, 4 – Luojiashan hill.
Fig. 4. 1, 2 in Heterotrophic Flagellates from Freshwater and Soil Habitats in Subtropical China (Wuhan Area, Hubei Province)
Fig. 4. 1, 2 – Petalomonas minuta (small cell with single anterior flagellum and longitudinal groove); 3, 4 – P. pusilla (small cell with single anterior flagellum and truncate anterior end); 5–7 – Phalansterium sp. (colonies of unikont spherical cell surrounded by mucilage); 8–12 – Phyllomitus apiculatus (cells with visible flagellar pocket, two heterodynamic flagella, anterior flagellum curves back over the rostrum (8), big food vacuoles), (12) whole mount (TEM); 13, 14 – Protaspa simplex (gliding spherical cells, cell body wags in unison with the flagellar beat); 15, 16 – Pteridomonas pulex (single apical flagellum emerging from a slight depression at the top of the cell, flagellum is surrounded by 12 stiffarms, body attaches to substrate by thin stalk); 17–19 – Rhynchomonas nasuta (oval cell bears undulating proboscis and long posterior flagellum), (19) whole mount (TEM); 20, 21 – Salpingoeca amphoridium (cell with narrow neck inside amphora-like lorica); 22 – S. gracilis (cylindrical cell inside cyathiform lorica); 23–25 – S. minor (spherical cell with narrow neck inside round lorica); 26–29 – Spongomonas uvella, (spherical cells with two isokont long acronematic flagella form colonies surrounded minute granules) (29) whole mount (TEM). Scale bars: 4 µm (3, 4), 5 µm (18, 23–25, 28, 29), 6 µm (1, 2), 8 µm (5, 7, 17, 19), 10 µm (6, 8–10, 12–14, 20, 27), 15 µm (11, 15, 21, 22, 26), 25 µm (16).
Figure 6 in Comparison of microplankton heterotrophic-photoautotrophic balance based on the content of ATP and chlorophyll a in the plankton of the northern area of the Black Sea during the autumn and spring seasons
Figure 6. Distribution of microplankton HPI in the photic zone of the Crimean coastal waters and deep-water northern part of the Black Sea at April 2017.
Figure 4 in Comparison of microplankton heterotrophic-photoautotrophic balance based on the content of ATP and chlorophyll a in the plankton of the northern area of the Black Sea during the autumn and spring seasons
Figure 4. Distribution of microplankton HPI in the photic zone of the Crimean coastal waters and deep-water northern part of the Black Sea at October 2016.
Figure 3 in Comparison of microplankton heterotrophic-photoautotrophic balance based on the content of ATP and chlorophyll a in the plankton of the northern area of the Black Sea during the autumn and spring seasons
Figure 3. Distribution of microplankton HPI in the surface waters of the Crimean coastal waters and deep-water northern part of the Black Sea at October 2016.
Figure 1 in Comparison of microplankton heterotrophic-photoautotrophic balance based on the content of ATP and chlorophyll a in the plankton of the northern area of the Black Sea during the autumn and spring seasons
Figure 1. Distribution of microplankton chlorophyll a and ATP concentrations in the Crimean coastal waters and deepwaternorthern part of the Black Sea at October 2016.
Glacial meltwater determines the balance between autotrophic and heterotrophic processes in a Greenland fjord
<p>Raw data for the summer CTD transect, the annual CTD mooring, data from the seasonal sediment trap, data from the oxygen and 14C incubations and nutrients data presented in the paper</p>
Data for "Symbiotic nutrient cycling enables the long-term survival of Aiptasia in the absence of heterotrophic food sources"
<p>Supplementary figures and raw data associated with the publication "Symbiotic nutrient cycling enables the long-term survival of Aiptasia in the absence of heterotrophic food sources". Data for physiological and NanoSIMS measurements are uploaded as individual sheets/tabs in the .xslx file. </p> <p>"Fig. 1" contains data for physiological measurements (biomass, protein content, and symbiont density) of fed and starved Aiptasia. </p> <p>"Fig. 2" contains data for NanoSIMS measurements for regions of interest from the tissue of fed and starved Aiptasia as well as unlabelled control Aiptasia. </p> <p>The R script contains all code required to repeat the data analysis and plotting.</p> <p> </p>
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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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
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