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Fig. 2 in Range expansion of the invasive Tropical House Gecko, Hemidactylus mabouia (Squamata: Gekkonidae), in South America

Fig. 2. Dorsal views of adult male Hemidactylus mabouia (CORBIDI 6276) collected in Loreto (Genaro Herrera, Requena Province), Peru (A). Dorsal view of juvenile Hemidactylus mabouia (CORBIDI 15363) collected in Lima (Surquillo, Lima Province), Peru (B). Lateral view of body (C) and head (D), ventral view of head and body (E), and ventral view of right hand (F) of the same individual (CORBIDI 15363). Photographs by Pablo Venegas (A) and Germán Chávez (B–F).

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Fig. 3 in Range expansion of the invasive Tropical House Gecko, Hemidactylus mabouia (Squamata: Gekkonidae), in South America

Fig. 3. Dorsolateral views of adult Hemidactylus frenatus from Aur Island, Malaysia (A), Nam Du Island, Vietnam (B), and Villavicencio, Meta, Colombia (C–D). Photographs by L. Lee Grismer (A–B) and Juan D. Vásquez-Restrepo (C–D).

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Changes in four decades of near-CONUS tropical cyclones in an ensemble of 12km thermodynamic global warming simulations

<p>Snapshot level data of TC extractions from the thermodynamical global warming runs described in "Changes in four decades of near-CONUS tropical cyclones in an ensemble of 12km thermodynamic global warming simulations."</p>

Fig. 7. The relationship between antenna 1 in The Distinctive Species Characteristics Of Metaprotella Sandalensis Mayer, 1898 (Crustacea: Amphipoda), Commonly Distributed Throughout The Tropical West Pacific Coasts

Fig. 7. The relationship between antenna 1 length and body length of Metaprotella sandalensis collected from coastal areas of Lifou Island.

Fig. 4 in The Distinctive Species Characteristics Of Metaprotella Sandalensis Mayer, 1898 (Crustacea: Amphipoda), Commonly Distributed Throughout The Tropical West Pacific Coasts

Fig. 4. Metaprotella sandalensis, female, 5.03 mm, AM P.87576, Pointe de Easo (= Easho), Baie de Sandal, Lifou Island. Scales for G1 and G2 represent 0.1 mm; A1, A2, and whole body represent 0.2 mm.

Fig. 3 in The Distinctive Species Characteristics Of Metaprotella Sandalensis Mayer, 1898 (Crustacea: Amphipoda), Commonly Distributed Throughout The Tropical West Pacific Coasts

Fig. 3. Metaprotella sandalensis, male, 8.87 mm, AM P.87572, Pointe de Easo (= Easho), Baie de Sandal, Lifou Island. Scales for ABD (L) and ABD (V) represent 0.05 mm; P3 and P4 represent 0.1 mm; P5 and P7 represent 0.2 mm.

Fig. 5 in The Distinctive Species Characteristics Of Metaprotella Sandalensis Mayer, 1898 (Crustacea: Amphipoda), Commonly Distributed Throughout The Tropical West Pacific Coasts

Fig. 5. Metaprotella sandalensis, female, 5.03 mm, AM P.87576, Pointe de Easo (= Easho), Baie de Sandal, Lifou Island. All scales represent 0.05 mm.

Fig. 6 in The Distinctive Species Characteristics Of Metaprotella Sandalensis Mayer, 1898 (Crustacea: Amphipoda), Commonly Distributed Throughout The Tropical West Pacific Coasts

Fig. 6. Metaprotella sandalensis, female, 5.03 mm, AM P.87576, Pointe de Easo (= Easho), Baie de Sandal, Lifou Island. Scales for ABD (L) and ABD (V) represent 0.05 mm; P3, P4, P5, P6, and P7 represent 0.1 mm.

Fig. 2 in The Distinctive Species Characteristics Of Metaprotella Sandalensis Mayer, 1898 (Crustacea: Amphipoda), Commonly Distributed Throughout The Tropical West Pacific Coasts

Fig. 2. Metaprotella sandalensis, male, 8.87 mm, AM P.87572, Pointe de Easo (= Easho), Baie de Sandal, Lifou Island. All scales represent 0.05 mm.

Fig. 1 in The Distinctive Species Characteristics Of Metaprotella Sandalensis Mayer, 1898 (Crustacea: Amphipoda), Commonly Distributed Throughout The Tropical West Pacific Coasts

Fig. 1. Metaprotella sandalensis, male, 8.87 mm, AM P.87572, Pointe de Easo (= Easho), Baie de Sandal, Lifou Island. Scales for A1, G1, and HD represent 0.1 mm; A2 and G2 represent 0.2 mm; whole body represents 0.5 mm.

Fig. 4 in Characterization of the Plasmodium and Haemoproteus parasite community in temperate-tropical birds during spring migration

Fig. 4. Differences by foraging guild among infected birds in the probability of Haemoproteus versus Plasmodium infection adjusted for the significant predictors in the model. Single asterisks with brackets beneath denote significant differences between categories.

Fig. 3 in Characterization of the Plasmodium and Haemoproteus parasite community in temperate-tropical birds during spring migration

Fig. 3. Differences by wintering ground among infected birds in the probability of Haemoproteus versus Plasmodium infection adjusted for the significant predictors in the model. Single asterisks with brackets beneath denote significant differences between categories.

Fig. 2 in Characterization of the Plasmodium and Haemoproteus parasite community in temperate-tropical birds during spring migration

Fig. 2. Differences by avian family in the probabilities of a) infection versus non-infection with a Haemosporidian parasite and b) among infected birds, the Plasmodium versus Haemoproteus infection adjusted for the significant predictors in the respective models. Single asterisks with brackets beneath denote significant differences between families.

Fig. 1 in Characterization of the Plasmodium and Haemoproteus parasite community in temperate-tropical birds during spring migration

Fig. 1. Location of field site in Clive Runnells Family Mad Island Marsh Preserve in Texas, USA (Image credit: Google Earth).

Fig. 8 in Does dredging activity exert an influence on benthic macrofauna in tropical estuaries? Case study on the northern coast of Brazil

Fig. 8. Diagram of Principal Component Analysis during collection periods [Temp(W), water temperature; Sal(W), water salinity; OD(W), water dissolved oxygen; pH(W), pH of water; Fe(W), water iron; Mn(W), water manganese; Cu(S), copper from sediment; Cr(S), chromium from sediment; Ni(S), nickel from sediment; Zn(S), zinc from sediment].

Fig. 7 in Does dredging activity exert an influence on benthic macrofauna in tropical estuaries? Case study on the northern coast of Brazil

Fig. 7. Dendrogram of Bray-Curtis similarity between the points sampled in the Port Complex of SÃo LuÍs, MaranhÃo, Brazil.

Fig. 3 in Does dredging activity exert an influence on benthic macrofauna in tropical estuaries? Case study on the northern coast of Brazil

Fig. 3. Temporal and spatial variation of different granulometric size fractions contribution (%) to the sediment total weight at SÃo LuÍs Harbor, MaranhÃo, Brazil. The number below the x-axis indicate the sampling stations.

Fig. 6 in Does dredging activity exert an influence on benthic macrofauna in tropical estuaries? Case study on the northern coast of Brazil

Fig. 6. Number of species, density and diversity of Shannon of the benthic macrofauna found in the Port Complex of SÃo LuÍs, MaranhÃo, Brazil: (A) Number of species, (B) Density, (C) Shannon diversity and (D) Lumbrineris sp.

Fig 5 in Does dredging activity exert an influence on benthic macrofauna in tropical estuaries? Case study on the northern coast of Brazil

Fig 5. Temporal and spatial variation of metals and semimetals concentrations (mg kg-1) in the sediment at SÃo LuÍs Harbor, MaranhÃo, Brazil: (A) Lead, (B) Copper, (C) Chrome, (D) Nickel, (E) Zinc and (F) Arsenic.

Fig. 2 in Does dredging activity exert an influence on benthic macrofauna in tropical estuaries? Case study on the northern coast of Brazil

Fig. 2. Temporal and spatial variation of sub superficial salinity (A), temperature (B), dissolved oxygen (C) and pH (D) at SÃo LuÍs Harbor, MaranhÃo, Brazil.