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517 results for “Floodplain”

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Figure 2 from: Ferreira GS, Almeida dos Santos DA, Lopes EV (2019) Richness, abundance and microhabitat use by Ardeidae (Aves: Pelecaniformes) during one seasonal cycle in the floodplain lakesof the lower Amazon River. Zoologia 36: 1-10. https://doi.org/10.3897/zoologia.36.e30475

Figure 2 Sampling design for macrofauna collection in the intertidal zone. Each station included three pooled samplings per strata (upper, middle and lower) of the intertidal zone as sampling unit.

opencc-by-4.0Oct 2019View details →
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Figure 1 from: Ferreira GS, Almeida dos Santos DA, Lopes EV (2019) Richness, abundance and microhabitat use by Ardeidae (Aves: Pelecaniformes) during one seasonal cycle in the floodplain lakesof the lower Amazon River. Zoologia 36: 1-10. https://doi.org/10.3897/zoologia.36.e30475

Figure 1 Map of the study area showing Grussaí Beach and Manguinhos Beach, in northern Rio de Janeiro, Brazil.

opencc-by-4.0Oct 2019View details →
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Text-fig. 2 Photos of palynomorphs. AP: 1.-2. Picea (B4-2, depth 0.35 m), 3.-4. Abies (B9, depth 0.10 m, B11-3, depth 0.01 m), 5.-8. Pinus (B8, depth 0.15 m, B9, depth 0.10 m), 9.-11. Alnus (B8, depth 0.15 m, B11, depth 0.01 m), NAP: 16.-17. Asteraceae Liguliflorae (B4-2, depth 0.35 m), 18.-20. Cyperaceae (B9, depth 0.10 m, B11-3, depth 0.01 m), 21.-22. Artemisia (B8, depth 0.15 m), Pteridophyta: 23.-26. Polypodiaceae (B4-2, depth 0.35 m, B8, depth 0.15 m), 27.-28. Equisetum (B7, depth 0.20 m), 29.-30. Sphagnum (B4-2, depth 0.35 m). Photo E. Břízová. in Reconstruction Of Vegetation Development On The Floodplain Of The Litavka River In The Holocene (Central Bohemia, Brdy Mts.)

Text-fig. 2 Photos of palynomorphs. AP: 1.-2. Picea (B4-2, depth 0.35 m), 3.-4. Abies (B9, depth 0.10 m, B11-3, depth 0.01 m), 5.-8. Pinus (B8, depth 0.15 m, B9, depth 0.10 m), 9.-11. Alnus (B8, depth 0.15 m, B11, depth 0.01 m), NAP: 16.-17. Asteraceae Liguliflorae (B4-2, depth 0.35 m), 18.-20. Cyperaceae (B9, depth 0.10 m, B11-3, depth 0.01 m), 21.-22. Artemisia (B8, depth 0.15 m), Pteridophyta: 23.-26. Polypodiaceae (B4-2, depth 0.35 m, B8, depth 0.15 m), 27.-28. Equisetum (B7, depth 0.20 m), 29.-30. Sphagnum (B4-2, depth 0.35 m). Photo E. Břízová.

opencc-by-4.0Dec 2008View details →
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Fig. 1 in Association of Anagrus amazonensis Triapitsyn, Querino & Feitosa (Hymenoptera, Mymaridae) with aquatic insects in upland streams and floodplain lakes in central Amazonia, Brazil

Fig. 1. Sites where Anagrus amazonensis (Hymenoptera, Mymaridae), its hosts, and their associated plants were collected in Amazonas State, Brazil.

opencc-by-4.0May 2016View details →
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FIGURE 1. A in Cymbopleura laszlorum spec. nov. (Cymbellaceae, Bacillariophyceae), a glacial relic from a calcium-rich floodplain fen in southwestern Montana, USA

FIGURE 1. A spring-fed pool on the Granger Ranch fen. Photo by Tara Luna.

opennotspecifiedMay 2018View details →
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FIGURE 32–47 in Two new diatom species (Bacillariophyceae) from Brazilian floodplain: Actinella hermes-moreirae sp. nov. and Gomphonema mutunensis sp. nov.

FIGURE 32–47. Gomphonema mutunensis sp. nov. LM. Valve view from type material. Scale bar = 10 μm.

opennotspecifiedMar 2019View details →
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FIGURE 1 in Eunotia Ehrenberg (Eunotiaceae, Bacillariophyta) in a subtropical floodplain: a new species and taxonomic contributions

FIGURE 1. Study area in the Upper Paraná River Floodplain showing the Garças and Patos lakes.

opennotspecifiedMay 2021View details →
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Fig. 3 in Effects of flood regime on the diet of Triportheus curtus (Garman, 1890) in an Amazonian floodplain lake

Fig. 3. Scores derived from Detrended Correspondence Analysis (DCA), considering the seasonal ordination of Triportheus curtus in the periods of the hydrological cycle of Lake Amapá.

opencc-by-4.0Sep 2011View details →
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Fig. 4 in Effects of flood regime on the diet of Triportheus curtus (Garman, 1890) in an Amazonian floodplain lake

Fig. 4. Mean values for scores (± standard error) for axes 1 (a) and 2 (b) of the detrended correspondence analysis (DCA), in the different sampling periods.

opencc-by-4.0Sep 2011View details →
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Fig. 5 in Stability and spatio-temporal structure in fish assemblages of two floodplain lagoons of the lower Orinoco River

Fig. 5. Variability by hydrological phases and habitats of the diversity and equitability (Shanon) and richness. a and b = the Arhuacas; c and d = the Cardonales. 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. 1 in Fish larvae assemblages in two floodplain lakes with different degrees of connection to the Paraná River, Brazil

Fig. 1. Locations of the sampling sites in Ilha Grande National Park, upper Paraná River. X1 - Xambrê stream; X2 - Xambrê middle; S1 - Saraiva channel; and S2- Saraiva middle.

opencc-by-4.0Sep 2009View details →
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Fig. 3 in Fish larvae assemblages in two floodplain lakes with different degrees of connection to the Paraná River, Brazil

Fig. 3. Variations in mean fish larvae abundance 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. 1 in Comparative feeding ecology and habitats use of Crenicichla species (Perciformes: Cichlidae) in a Venezuelan floodplain river

Fig. 1. Specimens of (a) Crenicichla lugubris (217 mm SL) and (b) C. aff. wallacii (51 mm SL) from the Cinaruco River, Venezuela.

opencc-by-4.0Jun 2009View details →
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Fig. 7 in Ecology and life history of an Amazon floodplain cichlid: the discus fish Symphysodon (Perciformes: Cichlidae)

Fig. 7. Length vs. weight plots for Symphysodon haraldi specimens parasitized with the isopod gill parasite Braga cichlae, and unparasitized specimens. All specimens are from a single colony of discus in Uxi Bay, lago Amanã.

opencc-by-4.0Dec 2008View details →
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Fig. 4 in Ecology and life history of an Amazon floodplain cichlid: the discus fish Symphysodon (Perciformes: Cichlidae)

Fig. 4. (right column) Testes and ovaries of Symphysodon haraldi at advancing stages of gonadal development. Photographs are from freshly sacrificed and dissected specimens, with the gonads outlined for clarity. The following modified version of Nikolsky's scale of reproductive maturity was utilized: 0. (immature): gonads thin and transparent; sex determination not possible (not illustrated). 1. (early development or resting): testes thin and translucent; ovaries thin and translucent-pink with transparent eggs. 2. (maturing): testes translucent white; ovaries enlarged with white eggs. 3. (mature): testes thick and white; ovaries enlarged with largest eggs yellow. 4. (pre-spawning): testes swollen and sperm-positor everted; ovaries swollen with largest eggs orange, swollen and approximately 1.4 mm in diameter, ovipositor everted. 5. (spent): testes flaccid; ovaries flac- cid with scattered eggs of various size classes (not illustrated).

opencc-by-4.0Dec 2008View details →
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Fig. 2 in Ecology and life history of an Amazon floodplain cichlid: the discus fish Symphysodon (Perciformes: Cichlidae)

Fig. 2. (a) Flood level and (b) electrical conductivity (EC) monitored in lago Amanã during the period 1995-1998. The timing of sampling in Uxi Bay is marked by A (1998) and B (1997). Dotted horizontal lines mark where shore-scrub (4m) and higher portions of blackwater igapó forest (10m) are inun- dated (Fig. 1). Dotted circles are speculated spawning events for the putative cohort groups 1a through 3 (refer to Fig. 8).

opencc-by-4.0Dec 2008View details →
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Figs. 2a-d in Factors influencing Serrapinnus notomelas (Characiformes: Characidae) populations in upper Paraná river floodplain lagoons

Figs. 2a-d. Temporal variation in the abundance of Serrapinnus notomelas in lagoons Capivara (a), Clara (b), Pousada (c) and Traíra (d).

opencc-by-4.0Mar 2006View details →
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Fig. 3 in Fish assemblages of tropical floodplain lagoons: exploring the role of connectivity in a dry year

Fig. 3. Average values (± standard error) of species richness (a), density (b), and biomass (c) in connected () and disconnected () lagoons.

opencc-by-4.0Dec 2003View details →
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Figure 6 from: Loughman Z, Simon T (2011) Zoogeography, taxonomy, and conservation of West Virginia's Ohio River floodplain crayfishes (Decapoda, Cambaridae). ZooKeys 74: 1-78. https://doi.org/10.3897/zookeys.74.808

Figure 6 - Cambarus carinirostris and Cambarus bartonii cavatus distribution along the West Virginia portion of the Ohio River floodplain

opencc-by-4.0Jan 2011View details →
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Figure 2 from: Loughman Z, Simon T (2011) Zoogeography, taxonomy, and conservation of West Virginia's Ohio River floodplain crayfishes (Decapoda, Cambaridae). ZooKeys 74: 1-78. https://doi.org/10.3897/zookeys.74.808

Figure 2 - Ohio River floodplain collection sites – Northern Counties. Site numbers correspond to numbers in Table 1.

opencc-by-4.0Jan 2011View details →

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