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517 results for “Floodplain”

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Figures 1–4 in The freshwater medusa Limnocnida and associated plankton in the floodplain of the Ayeyarwaddy River, Myanmar

Figures 1–4. Limnocnida from Myanmar. (1) Whole umbrella showing primary tentacles on one quadrant, and all tentacles on another quadrant. (2) Umbrella margin, showing bases of two primary tentacles with associated secondary tentacles and statocysts. (3) Part of the basal region of a tentacle showing groups of nematocysts. (4) Arrangement of nematocysts near the tip of a tentacle.

opencc-by-4.0May 2005View details →
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Fig. 2 in Effects of flood regime on the diet of Triportheus curtus (Garman, 1890) in an Amazonian floodplain lake

Fig. 2. Variation in river level (measured every three days) during the hydrological cycle from 2008 to 2009 in Lake Amapá. Gray line shows the threshold level for flooding from the Acre River. Main periods of pre-flooding, flooding, and postflooding are indicated at the base of the graph.

opencc-by-4.0Sep 2011View details →
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Fig. 7. a in Ecomorphological patterns of the fish assemblage in a tropical floodplain: effects of trophic, spatial and phylogenetic structures

Fig. 7. a) Diagram of Canonical Discriminant Analysis for the ecomorphological indices of the fish assemblage grouping in habitat types in the upper Paraná River floodplain (rivers, channels, connected and disconnected lagoons). b) Histograms with the scores of the habitat types for Canonical axis 1.

opencc-by-4.0Dec 2010View details →
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Fig. 6 in Ecomorphological patterns of the fish assemblage in a tropical floodplain: effects of trophic, spatial and phylogenetic structures

Fig. 6. Diagram of Canonical Discriminant Analysis for the ecomorphological indices of the fish assemblage grouping in trophic guilds in the upper Paraná River floodplain (detritivores, insectivores, piscivores, invertivores, omnivores and herbivores).

opencc-by-4.0Dec 2010View details →
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Fig. 4 in Ecomorphological patterns of the fish assemblage in a tropical floodplain: effects of trophic, spatial and phylogenetic structures

Fig. 4. Distribution of scores centroids of the 35 species on the first two axes of the Principal Components Analysis (PC 1 and PC 2), applied to the correlation matrix (Pearson) formed by 22 ecomorphological indices. Each polygon defines the morphological space occupied by the species that compose the corresponding trophic guild.

opencc-by-4.0Dec 2010View details →
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Fig. 5 in Ecomorphological patterns of the fish assemblage in a tropical floodplain: effects of trophic, spatial and phylogenetic structures

Fig. 5. Distribution of scores centroids of the 35 species grouped by habitat type on the first two axes of the Principal Components Analysis (PC 1 and PC 2), applied to the correlation matrix (Pearson) formed by 22 ecomorphological indices. Each polygon defines the morphological space occupied by the species that exploit the corresponding habitat type.

opencc-by-4.0Dec 2010View details →
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Fig. 3 in Ecomorphological patterns of the fish assemblage in a tropical floodplain: effects of trophic, spatial and phylogenetic structures

Fig. 3. Distribution of scores centroids of the 35 species on the first two axes of the Principal Components Analysis (PC 1 and PC 2), applied to the correlation matrix (Pearson) formed by 22 ecomorphological indices.

opencc-by-4.0Dec 2010View details →
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Fig. 2 in Ecomorphological patterns of the fish assemblage in a tropical floodplain: effects of trophic, spatial and phylogenetic structures

Fig. 2. Schematic representation of the linear morphometric measurements and the calculated areas: standard length (SL), maximum body height (MBH), body midline height (BMH), maximum body width (MBW), caudal peduncle length (CPdL), caudal peduncle height (CPdH), caudal peduncle width (CPdW), head length (HdL), head height (HdH), head width (HdW), length of snout with the mouth closed (LSC), length of snout with the mouth open (LSO), eye height (EH), mouth height (MH), mouth width (MW), dorsal fin length (DL), dorsal fin height (DH), caudal fin length (CL), caudal fin height (CH), anal fin length (AL), anal fin height (AH), pectoral fin length (PtL), pectoral fin height (PtH), pelvic fin length (PvL), pelvic fin height (PvH), eye area (EA), dorsal fin area (DA), caudal fin area (CA), anal fin area (AA), pectoral fin area (PtA), and pelvic fin area (PvA).

opencc-by-4.0Dec 2010View details →
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Fig. 1 in Ecomorphological patterns of the fish assemblage in a tropical floodplain: effects of trophic, spatial and phylogenetic structures

Fig. 1. Study area with sampling stations in the upper Paraná River floodplain: rivers: Paraná (1), Baía (2) and Ivinheima (3); channels: Cortado (4), Curutuba (5) and Ipoitã (6); connected lagoons: Garças (7), Guaraná (8) and Finado Raimundo (9); disconnected lagoons: Fechada (10), Ventura (11) and Zé do Paco (12).

opencc-by-4.0Dec 2010View details →
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Fig. 1 in Stability and spatio-temporal structure in fish assemblages of two floodplain lagoons of the lower Orinoco River

Fig. 1. Locations of the two studied lagoons in the right bank of the lower Orinoco river, between the cities of Puerto Ordaz and Ciudad Bolívar, Bolívar State, Venezuela. The arrows in black indicate the lagoons.

opencc-by-4.0Dec 2009View details →
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Fig. 3 in Stability and spatio-temporal structure in fish assemblages of two floodplain lagoons of the lower Orinoco River

Fig. 3. Percentage abundance of total species (S) and number of species for orders in each habitats of the lagoons. The abbreviations of the habitats are explained in the Fig. 2.

opencc-by-4.0Dec 2009View details →
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Fig. 4 in Stability and spatio-temporal structure in fish assemblages of two floodplain lagoons of the lower Orinoco River

Fig. 4. Mean values (+ confidence interval) of abundance, biomass and richness by habitats and hydrological phases between lagoons. The abbreviations of the hydrological phases and habitats are explained in the Fig. 2.

opencc-by-4.0Dec 2009View details →
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Fig. 6. nMDS analysis during high waters and low waters. a and b in Stability and spatio-temporal structure in fish assemblages of two floodplain lagoons of the lower Orinoco River

Fig. 6. nMDS analysis during high waters and low waters. a and b = gill nets sampling; c and d = seine net sampling. Each symbol represents one sample, filled symbols belongs to Las Arhuacas (arh) and those of open symbols to Los Cardonales (car). The dissimilarity between the sampling is approximately proportional to the distance, that is to say to greater distance greater dissimilarity. The abbreviations of the habitats are explained in the Fig. 2.

opencc-by-4.0Dec 2009View details →
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Fig. 2 in Stability and spatio-temporal structure in fish assemblages of two floodplain lagoons of the lower Orinoco River

Fig. 2. Percentage distribution abundance and biomass of fish by habitats in each hydrological phase in both lagoons. DW = Descent water, LW = Low water, RW = Raise water and HW = High water. RO = Rocky outcrops, FGF = Flooded grass fields, FF = Floodplain forests, B = Beach, AV = Aquatic vegetation, LZFT = Littoral zone with fallen trunks and LZOW = Littoral zone and open waters.

opencc-by-4.0Dec 2009View details →
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Fig. 2 in Fish larvae assemblages in two floodplain lakes with different degrees of connection to the Paraná River, Brazil

Fig. 2. Larvae abundances for the different species in Xambrê Lake (a) and Saraiva Lake (b) in Ilha Grande National Park, upper Paraná River, during the three studied spawning seasons.

opencc-by-4.0Sep 2009View details →
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Fig. 5 in Fish larvae assemblages in two floodplain lakes with different degrees of connection to the Paraná River, Brazil

Fig. 5. Sample scores of retained axes (Axes 1, 2, and 3) from the non-metric multidimensional scaling (NMS) controlling for sites (S1 - Saraiva channel, S2 - Saraiva middle, X1 - Xambrê stream and X2 - Xambrê middle) (a; b) and spawning seasons (I, II and III) (c; d). Variation of mean scores axis for sites (e) and spawning seasons (f) in Ilha Grande National Park, upper Paraná River (s.d. = standard deviation).

opencc-by-4.0Sep 2009View details →
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Fig. 4 in Fish larvae assemblages in two floodplain lakes with different degrees of connection to the Paraná River, Brazil

Fig. 4. Variations in mean species richness (number of species) (a), evenness (E) (b) and Shannon Diversity Index (H') (c) of fish larvae per sampling for Xambrê Lake and Saraiva Lake sites (S1 - Saraiva channel, S2 - Saraiva middle, X1 - Xambrê stream and X2 - Xambrê middle) in Ilha Grande National Park, upper Paraná River, during the three studied spawning seasons (s.d. = standard deviation).

opencc-by-4.0Sep 2009View details →
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Fig. 3 in Relationships between water transparency and abundance of Cynodontidae species in the Bananal floodplain, Mato Grosso, Brazil

Fig. 3. Cluster dendrogram based on relative abundance in biomass of Cynodontidae species and water transparency from 15 sampling sites in the Bananal floodplain, Mato Grosso, Brazil (UPGMA algorithm, Euclidian distance). See Table 1 for site codes.

opencc-by-4.0Jun 2009View details →
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Fig. 1 in Relationships between water transparency and abundance of Cynodontidae species in the Bananal floodplain, Mato Grosso, Brazil

Fig. 1. Partial map of South America showing the location of the study area in the Bananal floodplain. The detailed map depicts the sampling sites (circles) in the rios Araguaia and Mortes basins. See Table 1 for site codes.

opencc-by-4.0Jun 2009View details →
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Fig. 2 in Relationships between water transparency and abundance of Cynodontidae species in the Bananal floodplain, Mato Grosso, Brazil

Fig. 2. Linear regression between relative abundance in biomass (a) and number of individuals (b) of Cynodontidae species and water transparency from 15 sampling sites in the Bananal floodplain, Mato Grosso, Brazil.

opencc-by-4.0Jun 2009View details →

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