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325 results for “Brackish water”
Figure 5 in AfriBasins: a new framework in FishBase for the analysis of African fresh and brackish water fish distributions, with a discussion on the Congo basin fauna
Figure 5. – Cluster analysis on the fish distribution data for the Congo Basin s.s., based on (A) the Ochiai coefficient and (B) the correlation ratio.
Figure 7 in AfriBasins: a new framework in FishBase for the analysis of African fresh and brackish water fish distributions, with a discussion on the Congo basin fauna
Figure 7. – Evolution of the estimated number of species based on various definitions of the Congo basin: Central Congo, i.e. Kinshasa to Kisangani, without Kasai upstream from Mushie (Poll and Gosse, 1963); without lakes Bangweulu and Mweru (Roberts, 1972); entire Congo (Poll, 1973); excluding Lake Tanganyika (Lowe-McConnell, 1987); excluding lakes Tanganyika and Mweru, primary freshwater species (Teugels and Guégan, 1994); Zaïre, probably only includes primary freshwater species (Lévêque, 1997); Zaïre, probably includes primary, secondary and peripheral species (Lévêque, 1997); Congo River system, at least 700 species (Skelton, 2001); Congo and Lake Tanganyika (Revenga and Kura, 2003); Congo River system (Thieme et al., 2005); the Congo (Dumont, 2009); Congo basin including the Rift Valley region with lakes Tanganyika and Kivu and the Malagarasi basin (Snoeks et al., 2011).
Figure 1 in Quantum yield, chlorophyll, and cell damage in yellow passion fruit under irrigation strategies with brackish water and potassium
Figure 1. Data of precipitation, maximum and minimum air temperatures, and relative humidity of air observed during the experimental period.
Figure 3 in Quantum yield, chlorophyll, and cell damage in yellow passion fruit under irrigation strategies with brackish water and potassium
Figure 3. Electrolyte leakage - % IEL (A) and relative water content - RWC (B) of yellow passion fruit plants 'BRS GA1' as a function of the interaction between the use of brackish water irrigation strategies and potassium doses at 445 and 360 days after transplanting, respectively. Vertical bars represent the standard error of mean (n = 4). Means followed by the same lowercase letters indicate no significant difference between management strategies by the Scott-Knott test (p≤0.05) for the same potassium dose, and the same uppercase letters indicate no significant difference between potassium doses by the Tukey test (p ≤ 0.05) for the same strategy. For details of BWIS see Table 4.
Fig. 1 in Morphological reports of four ciliates (Ciliophora) from coastal marine and brackish water habitats in Korea
Fig. 1. Photomicrographs of four ciliates on the basis of live observation (A, C, E, H) and after protargol impregnation (B, D, F, G, I). A, B, Gruberia calkinsi, left side view of a living specimen (A) and right side view of a protargolimpregnated specimen (B); C, D, Dysteria crassipes, left side views of living (C) and protargolimpregnated (D) specimens; EG, Zosterodasys agamaliev, ventral view of a living specimen (E), and ventral (F) and dorsal (G) views of potargolimpregnated specimens; H, I, Pleuronema salmastra, ventral views of living (H) and protargolimpregnated (I) specimens. Scale bars: A = 500 μm, B = 300 μm, C, D = 30 μm, E, H = 50 μm.
Fig. 7 in Testate Amoebae as Proxy for Water Level Changes in a Brackish Tidal Marsh
Fig. 7. Graphs of observed versus estimated Elevation and Normalized elevation, predicted by the transfer function based on Jack-knifed WA-PLS (component 2) for the complete dataset, after the removing of outliers and for the partial dataset.
Fig. 1. A in Testate Amoebae as Proxy for Water Level Changes in a Brackish Tidal Marsh
Fig. 1. A – map of the Scheldt estuary with location of Groot Buitenschoor; B – map of the brackish tidal marsh Groot Buitenschoor with indication of vegetation zones and the elevation transects that are sampled; C – photos of the two sampled transects. Photo 1 – from Salix to outer edge of Phragmites australis vegetation; Photo 2 – from Phragmites australis to outer edge of Scirpus maritimus.
Fig. 6 in Testate Amoebae as Proxy for Water Level Changes in a Brackish Tidal Marsh
Fig. 6. Results of the partial RDA for both intertidal (zone B) and supratidal (zone A) bio-zones. The values in the intersection of the circle are the common variation explained by the two variables.
Figure. The phylogenetic tree showing the relationship among Brevibacillus parabrevis strains SA2.2 and TJ2.3, Bacillus licheniformis MG4.2, and their phylogenetically closest type strains. The GenBank accession numbers of the type strains and studied strains are shown following species names. Distance matrix was calculated by Kimura's 2-parameter model. The scale bar indicates 0.02 substitutions per nucleotide position. Alicyclobacillus pohliae AJ564766 served as an out-group. in Distribution of extracellular enzyme-producing bacteria in the digestive tracts of 4 brackish water fish species
Figure. The phylogenetic tree showing the relationship among Brevibacillus parabrevis strains SA2.2 and TJ2.3, Bacillus licheniformis MG4.2, and their phylogenetically closest type strains. The GenBank accession numbers of the type strains and studied strains are shown following species names. Distance matrix was calculated by Kimura's 2-parameter model. The scale bar indicates 0.02 substitutions per nucleotide position. Alicyclobacillus pohliae AJ564766 served as an out-group.
Figure 4 in Does the location of coastal brackish waters determine diversity and abundance of zooplankton assemblages?
Figure 4. Seasonal (monthly) changes in the total zooplankton abundance (mean, minimum, and maximum densities) (ind. dm–3) in the Vistula Lagoon and Lake Łebsko in 2010–2011.
Figure 6 in Does the location of coastal brackish waters determine diversity and abundance of zooplankton assemblages?
Figure 6. Seasonal (monthly) changes in the total zooplankton biomass (mean, minimum, and maximum values) (mg. dm–3) in the Vistula Lagoon and Lake Łebsko in 2010–2011.
Linked collectors and determiners for: The occurrence, distribution and biology of invasive fish species in fresh and brackish water bodies of NE Morocco.
Natural history specimen data linked to collectors and determiners held within, "The occurrence, distribution and biology of invasive fish species in fresh and brackish water bodies of NE Morocco". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/55347db9-46a3-449d-8e55-ba6ed02e4820">https://bionomia.net/dataset/55347db9-46a3-449d-8e55-ba6ed02e4820</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/55347db9-46a3-449d-8e55-ba6ed02e4820">https://gbif.org/dataset/55347db9-46a3-449d-8e55-ba6ed02e4820</a>. Formatted as a Frictionless Data package.
FIG. 3 in A new species of Iravadia s.s. (Mollusca, Gastropoda, Iravadiidae) from the late Oligocene of the Aquitaine Basin (southern France). The earliest record of brackish-water Iravadiidae?
FIG. 3. — Iravadia (Iravadia) dolini n. sp., holotype; A, apertural view; B, abapertural view; C, right lateral view, height 3 mm.
FIG. 2 in A new species of Iravadia s.s. (Mollusca, Gastropoda, Iravadiidae) from the late Oligocene of the Aquitaine Basin (southern France). The earliest record of brackish-water Iravadiidae?
FIG. 2. — Iravadia (Iravadia) dolini n. sp.; A, protoconch of the paratype; B, abapical view of shell whorl sculpture, paratype; C-E, holotype, height 3 mm; C, apertural view; D, E, line drawings of the right lateral and abapertural views. Scale bars: A, B, 100 µm.
FIG. 1 in A new species of Iravadia s.s. (Mollusca, Gastropoda, Iravadiidae) from the late Oligocene of the Aquitaine Basin (southern France). The earliest record of brackish-water Iravadiidae?
FIG. 1. — Location of the fossil locality (), with the late Oligocene to mid-Miocene fill of the paleocanyon of Saubrigues (after Kieken 1973; Cahuzac et al. 1995).
FIG. 7 in Between Vanuatu tides: 3D anatomical reconstruction of a new brackish water acochlidian gastropod from Espiritu Santo
FIG. 7. — Transverse histological sections of Pseudunela espiritusanta n. sp.: A, pharynx with radula, penis, basal finger; B, salivary gland, buccal ganglion; C, sphincter; D, sperm storing receptacles. Abbreviations: am, ampulla; bf, basal finger; bg, buccal ganglion; ed, ejaculatory duct; gog, gastro-oesophageal ganglion; oe, oesophagus; p, penis; ph, pharynx; ppd, paraprostatic duct; pr, prostate; r, radula; rs, receptaculum seminis; s, sphincter; sgd, salivary gland duct; sgl, salivary gland; st, stylet of basal finger; vd, vas deferens. Scale bars: A-C, 100 μm; D, 25 μm.
FIG. 6 in Between Vanuatu tides: 3D anatomical reconstruction of a new brackish water acochlidian gastropod from Espiritu Santo
FIG. 6. — Reproductive system of Pseudunela espiritusanta n. sp. (schematic drawing). Abbreviations: alg, albumen gland; am, ampulla; bc, bursa copulatrix; bf, basal finger; do, oviduct; ed, ejaculatory duct; fgo, female gonopore;meg, membrane gland; mgo, male gonopore; mug, mucus gland; ov, ovotestis; p, penis; ppd, paraprostatic duct; ppr, paraprostate; pr, prostate; ps, penial sheath; pst, penial stylet; rs, receptaculum seminis; s, sphincter; st, stylet of basal finger; vd, vas deferens; vdp, posterior-leading vas deferens. Not to scale.
FIG. 5. — 3D in Between Vanuatu tides: 3D anatomical reconstruction of a new brackish water acochlidian gastropod from Espiritu Santo
FIG. 5. — 3D reconstruction of the circulatory, excretory and reproductive systems of Pseudunela espiritusanta n. sp.: A, circulatory and excretory systems, right view; B, complete reproductive system, dorsolateral view from right; C, nidamental glands, sperm storing receptacles and sphincter, right view; D, anterior male copulatory organs, left view. Abbreviations: alg, albumen gland; am, ampulla; ao, aorta; bc, bursa copulatrix; bf, basal finger; do, oviduct; ed, ejaculatory duct; h, heart; k, kidney; meg, membrane gland; mug, mucus gland; ndd, nephroduct dorsal branch; ndv, nephroduct ventral branch; np, nephropore; ov, ovotestis; p, penis; pc, pericardium; ppd, paraprostatic duct; ppr, paraprostate; pr, prostate; pst, penial stylet; rpd, renopericardioduct; rs, receptaculum seminis; s, sphincter; st, stylet of basal finger; vd, vas deferens; vdp, posterior-leading vas deferens. Scale bars: 200 μm.
FIG. 4 in Between Vanuatu tides: 3D anatomical reconstruction of a new brackish water acochlidian gastropod from Espiritu Santo
FIG. 4. — Radula of Pseudunela espiritusanta n. sp., SEM-micrographs: A, row of radular teeth; B, rhachidian teeth, right view; C, rhachidian tooth, anterior view; D, right lateral teeth, arrow points to blunt protrusion; E, left lateral teeth. Abbreviations: cc, central cusp; d, denticle; ltl, left lateral tooth; ltr1, first right lateral tooth; ltr2, second right lateral tooth; n, notch; 1-4, lateral denticle on rhachidian tooth. Scale bars: 10 μm.
FIG. 1 in Between Vanuatu tides: 3D anatomical reconstruction of a new brackish water acochlidian gastropod from Espiritu Santo
FIG. 1. — Habitat, external morphology and general anatomy of Pseudunela espiritusanta n. sp.: A, type locality when tide is just coming in; B, habitat of P. espiritusanta n. sp.: underside of rocks embedded in coarse sand (arrowhead points to exact place where specimens were found); C, 3D reconstruction, position of internal organs: green, central nervous system; blue/lilac, digestive system; yellow, circulatory and excretory systems; red/brownish, reproductive system; D, photograph of living specimen. Abbreviations: cns, central nervous system; dg, digestive gland; f, foot; k, kidney; lt, labial tentacle; ov, ovotestis; pr, prostate; rh, rhinophore; sgl, salivary gland; sp, spicule; vd, vas deferens; vh, visceral hump. Scale bars: C, 500 μm; D, 1 mm.
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Allen Brain Atlas
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