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Fig 9 in Four new species of Capsicum (Solanaceae) from the tropical Andes and an update on the phylogeny of the genus
Fig 9. Somatic metaphase chromosomes and ideogram of Capsicum piuranum. (A) Methaphase chromosomes. (B) Ideogram. Solid black blocks or dots denote CMA+/DAPI- (NOR) or CMA+/DAPIo (terminal and intercalary) heterochromatic bands. The NOR is indicated as a separate block. https://doi.org/10.1371/journal.pone.0209792.g009
Fig 8. Capsicum piuranum Barboza & S in Four new species of Capsicum (Solanaceae) from the tropical Andes and an update on the phylogeny of the genus
Fig 8. Capsicum piuranum Barboza & S. Leiva. (A) Plant. (B) Leaves, abaxial surface. (C) Fruiting branch. (D) Flower bud. (E) Flower and immature fruit. (F) Mature fruit. (G) Fruit, transverse section, showing placenta and seeds. (H) Fruit transverse section, showing a stone cell at the apex (arrow). Photos by S. Leiva González and G. E. Barboza. https://doi.org/10.1371/journal.pone.0209792.g008
Fig 5 in Four new species of Capsicum (Solanaceae) from the tropical Andes and an update on the phylogeny of the genus
Fig 5. Somatic metaphase chromosomes and ideogram of Capsicum longifolium. (A) Methaphase chromosomes. (B) Ideogram. Solid black blocks or dots denote CMA+/DAPI- (NOR) or CMA+/DAPIo (terminal and intercalary) heterochromatic bands. The NOR is indicated as a separate block. https://doi.org/10.1371/journal.pone.0209792.g005
Fig 12 in Four new species of Capsicum (Solanaceae) from the tropical Andes and an update on the phylogeny of the genus
Fig 12. Distribution of Capsicum neei Barboza & X. Reyes. https://doi.org/10.1371/journal.pone.0209792.g012
Figure 4 in Population Dynamics of Amoeboid Protists in a Tropical Desert: Seasonal Changes and Effects of Vegetation and Soil Conditions
Figure 4. Relationship between amoeboid protist richness and soil parameters during the wet season in three microhabitats by CCA: PL: Pr. laevigata, PP: Pa. praecox, and BS: bare soil. The names and abbreviations of the amoeboid protist species can be found in table 3.
Figure 2 in Population Dynamics of Amoeboid Protists in a Tropical Desert: Seasonal Changes and Effects of Vegetation and Soil Conditions
Figure 2. Cumulative richness plots of amoeboid protists present under Pr. laevigata (PL), Pa. praecox (PP) and bare soil (BS) during dry and wet seasons at 0–30 cm. a) eruptive pseudopods, and b) acanthopodial pseudopods. ND: not determined.
Figure 1 in Population Dynamics of Amoeboid Protists in a Tropical Desert: Seasonal Changes and Effects of Vegetation and Soil Conditions
Figure 1. Study area, showing vegetation patches in the desert of Tehuacán, Puebla, Mexico. In addition, the analyzed microhabitats are shown: Pr. laevigata, Pa. praecox and bare soil.
Fig. 3 in Fish diet composition in permanent and semi-permanent pools in tropical wetlands of the Yucatan Peninsula
Fig. 3. Percentage composition of main items consumed by fish in Permanent (A) and Semi-permanent (B) pools in BPR during the dry (black bars) and rainy season (dash bars) of 2010. FR = fish remains, TI = terrestrial invertebrates, AI = aquatic insects, PR = plant remains, CR = crustaceans (mainly amphipods), AR = arachnid, AL = algae, GA = gastropod and DE = detritus.
Fig. 2 in Fish diet composition in permanent and semi-permanent pools in tropical wetlands of the Yucatan Peninsula
Fig. 2. Fish feeding spectrum of aquatic insects and terrestrial invertebrates (proportions of different orders in the diet of all stomachs analyzed) between Permanent (A) and Semi-permanent (B) pools in the PBR during 2010. Species codes: Aa = Astyanax aeneus, Cu = Cichlasoma urophthalmus, Tm = Thorichthys meeki, Gy = Gambusia yucatana, Pv = Poecilia velifera, Pm = P. mexicana, Bb = Belonesox belizanus, Ro = Rocio octofasciata, Cs = Cichlasoma urophthalmus, Ps = Petenia splendida, On = Oreochromis niloticus, Pm = Paraneetroplus melanurus, Gp = Garmanella pulchra.
Fig. 1 in Fish diet composition in permanent and semi-permanent pools in tropical wetlands of the Yucatan Peninsula
Fig. 1. Geographic location of studied pools, permanent and semi-permanent in PBR, Campeche, Mexico during 2010.
Fig. 5 in Habitat preferences of common native fishes in a tropical river in Southeastern Brazil
Fig. 5. Substrate preferences of seven dominant native fish species in the Guandu River. Type of Substrate: 1, clay; 2, mud; 3, sand; 4, boulder/cobble/gravel; 5, bedrock.
Fig. 2 in Habitat preferences of common native fishes in a tropical river in Southeastern Brazil
Fig. 2. Distribution of sampling by habitat availability (%) in terms of depth (m), velocity (m s-1), and type of substrate. (1, clay; 2, mud; 3, sand; 4, boulder/cobble/gravel; 5, bedrock).
Fig. 1 in Habitat preferences of common native fishes in a tropical river in Southeastern Brazil
Fig. 1. Study area, Guandu River, indicating the four sampled stretches. WTP, Water Treatment Plant.
Figure 2 in First record of introduction of the tropical snail Melanoides tuberculata (O. F. Müller, 1774) in Bulgaria (Gastropoda: Thiaridae)
Figure 2. Shells of Melanoides tuberculata found at the thermal stream near Pancherevo. Scale bar 10 mm
Figure 1 in First record of introduction of the tropical snail Melanoides tuberculata (O. F. Müller, 1774) in Bulgaria (Gastropoda: Thiaridae)
Figure 1. The collection locality of Melanoides tuberculata – the thermal stream near Pancherevo Dam
FIGURE 1 in Ectoparasitic flies (Diptera, Streblidae) on bats (Mammalia, Chiroptera) in a dry tropical forest in the northern Colombia
FIGURE 1: Study sites of host-ectoparasite relationship between Streblidae and bats in Colombia. Darker areas correspond to higher altitudes.
Fig. 3 in Total mercury in the fish Trichiurus lepturus from a tropical estuary in relation to length, weight, and season
Fig. 3. Correlations (n = 104). a. Log weight (g) in respect to total length (cm); b. Log (mgHg-T.kg-1 in the muscle) in relation to total length (cm); c. Log (mgHg-T.kg-1) in relation to log weight (g) of Trichiurus lepturus from the Goiana Estuary from November 2005 to January 2007. All plots show a 95% confidence interval.
Fig. 2 in Total mercury in the fish Trichiurus lepturus from a tropical estuary in relation to length, weight, and season
Fig. 2. Rainfall in the study area from a historic (1961 to 1990) data set (solid line) and from 2005-2007 (bars). Source: http:// www.inmet.gov.br - meteorological station Recife-82.898).
Fig. 5 in Total mercury in the fish Trichiurus lepturus from a tropical estuary in relation to length, weight, and season
Fig. 5. Correlation (n = 81) between rainfall (mm) and log (µgHg-T.kg-1 in the muscle) of Trichiurus lepturus from the Goiana Estuary (1 = dry season 1 - November and December 2005, January 2006; 2 = end of the rainy season - August to October 2006; 3 = dry season 2 - November and December 2006, January 2007).
Fig. 3 in How does diet influence the reproductive seasonality of tropical freshwater fish? A case study of a characin in a tropical mountain river
Fig. 3. Non-Metric Multi-Dimensional Scaling Ordination (NMDS) of monthly variations of the diet with respect to sex. Stress = 0.10. Filled symbols are the dry months.
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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