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184 results for “freshwater habitat”
Figure 1 from: Shen H-W, Bao D-F, Hyde KD, Su H-Y, Bhat DJ, Luo Z-L (2021) Two novel species and two new records of Distoseptispora from freshwater habitats in China and Thailand. MycoKeys 84: 79-101. https://doi.org/10.3897/mycokeys.84.71905
Figure 1 Maximum likelihood (ML) tree is based on combined of LSU, ITS, SSU, TEF1-α, and RPB2 sequence data. Bootstrap support values with an ML greater than 70% and Bayesian posterior probabilities (PP) greater than 0.97 given above the nodes, shown as "ML/PP". The tree is rooted with Pseudostanjehughesia aquitropica (MFLUCC 16-0569) and P. lignicola (MFLUCC 15-0352). New species are indicated in red and type strains are in bold.
Figure 4 from: Shen H-W, Bao D-F, Hyde KD, Su H-Y, Bhat DJ, Luo Z-L (2021) Two novel species and two new records of Distoseptispora from freshwater habitats in China and Thailand. MycoKeys 84: 79-101. https://doi.org/10.3897/mycokeys.84.71905
Figure 4 Distoseptispora clematidis (KUN-HKAS 112708) A colonies on the substratum B-C conidiophores with conidia D conidiogenous cells E-H conidia I germinating conidium J culture on PDA Scale bars: 30 μm (B, C, E-I); 20 μm (D).
Figure 3 from: Shen H-W, Bao D-F, Hyde KD, Su H-Y, Bhat DJ, Luo Z-L (2021) Two novel species and two new records of Distoseptispora from freshwater habitats in China and Thailand. MycoKeys 84: 79-101. https://doi.org/10.3897/mycokeys.84.71905
Figure 3 Distoseptispora lancangjiangensis (KUN-HKAS 112712, holotype) A colonies on the substratum B conidiophore and conidium C-E conidiophores F, G conidiogenous cells H conidiogenous cell with conidium I-Q conidia R germinating conidium S, T culture on PDA. Scale bars: 50 μm (B-E); 20 μm (F-R).
Fig. 8 in Gill dimensions in near-term embryos of Amazonian freshwater stingrays (Elasmobranchii: Potamotrygonidae) and their relationship to the lifestyle and habitat of neonatal pups
Fig. 8. Dendrogram showing the association of freshwater stingrays based on the gill morphometry of the embryos.
Figure 2 from: Huang S-K, Jeewon R, Hyde KD, Bhat DJ, Chomnunti P, Wen T-C (2018) Beta-tubulin and Actin gene phylogeny supports Phaeoacremonium ovale as a new species from freshwater habitats in China. MycoKeys 41: 1-15. https://doi.org/10.3897/mycokeys.41.27536
Figure 2 Phaeoacremoniumovale (HKAS99550, holotype). a Substrate b, c Ascoma on host d Squashed neck e Ascoma in vertical section fPeridiumg Asci surrounded by paraphyses h Asci i Septate paraphyses j–m Asci with ascospores n Germinating ascospores. Note: Fig. i stained in Congo red reagent, fig l stained in Melzer's reagent. Scale bars: 500 µm (c); 200 µm (d); 100 µm (e); 50 µm (f, i); 30 µm (n); 20 µm (g–h); 10 µm (j–m)
Figure 1 from: Huang S-K, Jeewon R, Hyde KD, Bhat DJ, Chomnunti P, Wen T-C (2018) Beta-tubulin and Actin gene phylogeny supports Phaeoacremonium ovale as a new species from freshwater habitats in China. MycoKeys 41: 1-15. https://doi.org/10.3897/mycokeys.41.27536
Figure 1 Maximum likelihood phylogenetic tree generated from analysis of a combined TUB and ACT sequences dataset for 98 taxa of Togniniaceae. Pleurostomarichardsiae (CBS 270.33) and Wuestineaiamolokaiensis (CBS 114877) are the outgroup taxa. ML support values greater than 70% (BSML, left) and Bayesian posterior probabilities greater than 0.90 (BYPP, right) are indicated above the nodes. The strain numbers are noted after the species names. Ex-type strains are indicated in bold. Isolates from this study are indicated in red.
Figure 3 from: Huang S-K, Jeewon R, Hyde KD, Bhat DJ, Chomnunti P, Wen T-C (2018) Beta-tubulin and Actin gene phylogeny supports Phaeoacremonium ovale as a new species from freshwater habitats in China. MycoKeys 41: 1-15. https://doi.org/10.3897/mycokeys.41.27536
Figure 3 Phaeoacremoniumovale (HKAS99550, holotype). o Germinating ascospores, p 7 weeks of culture plate (above, left/reverse, right), q Mycelium with adelophialides r–t Branched conidiophores u–vConidia. Scale bars: 20 mm (p); 20 µm (o); 10 µm (r, t); 5 µm (q, s, u–v).
Figure 2 from: Gilbert H, Keany J, Culver DC (2018) Response of shallow subterranean freshwater amphipods to habitat drying. Subterranean Biology 28: 15-28. https://doi.org/10.3897/subtbiol.28.30700
Figure 2 Relative frequency of different behaviors of the three species in control (red bars) and experimental (blue bars).
Figure 1 in A new family of neotropical freshwater fishes from deep fossorial Amazonian habitat, with a reappraisal of morphological characiform phylogeny (Teleostei: Ostariophysi)
Figure 1. Tarumania walkerae gen. et sp. nov., holotype, INPA 33737.
Figure 2. The S in First record of scalloped hammerhead shark Sphyrna lewini (Carcharhiniformes: Sphyrnidae) in freshwater habitat
Figure 2. The S. lewini which stranded in Mahakam river at Muara Baroh village, Muara Pahu subdistrict, Kutai Barat district, East Kalimantan province (Photo: Yuni Sri Wahyuni).
Figure 8 in Microplastics in commercial fish digestive tracts from freshwater habitats in Northern Thailand
Figure 8. Comparison of abundance of plastics among fishes from different habitat groups (demersal, benthopelagic, and pelagic fishes).
Data from: Feasting in fresh water: impacts of food concentration on freshwater tolerance and the evolution of food x salinity response during the expansion from saline into fresh water habitats
Saline to freshwater invasions have become increasingly common in recent years. A key hypothesis is that rates of freshwater invasions have been amplified in recent years by increased food concentration, yet this hypothesis has remained unexplored. We examined whether elevated food concentration could enhance freshwater tolerance, and whether this effect evolves following saline to freshwater invasions. We examined physiological response to salinity and food concentration in a 2 × 2 factorial design, using ancestral brackish and freshwater invading populations of the copepod Eurytemora affinis. We found that high food concentration significantly increases low-salinity tolerance. This effect was reduced in the freshwater population, indicating evolution following the freshwater invasion. Thus, ample food could enable freshwater invasions, allowing subsequent evolution of low-salinity tolerance even under food-poor conditions. We also compared effects of food concentration on freshwater survival between two brackish populations from the native range. Impacts of food concentration on freshwater survival differed between the brackish populations, suggesting variation in functional properties affecting their propensity to invade freshwater habitats. The key implication is that high food concentration could profoundly extend range expansions of brackishwater species into freshwater habitats, potentially allowing for condition-specific competition between saline invaders and resident freshwater species.
Data from: Habitat effects on intra-species variation in functional morphology: evidence from freshwater fish
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Data from: Feasting in fresh water: impacts of food concentration on freshwater tolerance and the evolution of food x salinity response during the expansion from saline into fresh water habitats
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Data from: Apparent signal of competition limits diversification after ecological transitions from marine to freshwater habitats
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Chlorocladiella gen. nov., a new genus of Pithophoraceae (Cladophorales, Chlorophyta), including four new species from various freshwater habitats in China
<p>these three files descirbe 18S+28S rDNA alignments, 18S+28S+ITS rDNA alignments, and ITS2 secondary structure alignment respectively. </p>
Figure 1 from: Gilbert H, Keany J, Culver DC (2018) Response of shallow subterranean freshwater amphipods to habitat drying. Subterranean Biology 28: 15-28. https://doi.org/10.3897/subtbiol.28.30700
Figure 1 Average gravimetric soil moisture over the nine week trial.
Fig. 5 in Heterotrophic Flagellates from Freshwater and Soil Habitats in Subtropical China (Wuhan Area, Hubei Province)
Fig. 5. Species accumulation curve. Whiskers – standard deviation.
Data from: Phylogeography, historical demography, and habitat suitability modelling of freshwater fishes inhabiting seasonally fluctuating Mediterranean river systems: a case study using the Iberian cyprinid Squalius valentinus
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Figure 7 in A new family of neotropical freshwater fishes from deep fossorial Amazonian habitat, with a reappraisal of morphological characiform phylogeny (Teleostei: Ostariophysi)
Figure 7. Cranium of Tarumania walkerae, paratype, INPA 25747, 151.2-mm SL. (a) Dorsal view; (b) ventral view; (c) lateral view. Scale bar = 1 mm. ba, basioccipital; ep, epioccipital; ex, exoccipital; fr, frontal; le, lateral ethmoid; me, mesethmoid; os, orbitosphenoid; pa, parietal; par, parasphenoid; po, prootic; pt, pterotic; pts, pterosphenoid; so, supraoccipital; sph, sphenotic; vo, vomer.
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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.