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Fig. 4 in Daily activity patterns and occurrence of Leopardus guttulus (Carnivora, Felidae) in Lami Biological Reserve, southern Brazil

Fig. 4. Circular graph showing the distribution of Leopardus guttulus (Hensel, 1872) records in BRLJL, Rio Grande do Sul, Brazil, throughout the 12 months sampled. The black lines represent the concentration of records.

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Fig. 2 in Daily activity patterns and occurrence of Leopardus guttulus (Carnivora, Felidae) in Lami Biological Reserve, southern Brazil

Fig. 2. Circular graphs showing the daily activity of Leopardus guttulus (Hensel, 1872) at the BRLJL, Rio Grande do Sul, Brazil, based on all records obtained for the species (n=25, all seasons), on records obtained during spring/summer (n=15), and on records from autumn/winter (n=10). The arrow on each circular graphs indicates the direction of the angular mean.

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Fig. 1 in Daily activity patterns and occurrence of Leopardus guttulus (Carnivora, Felidae) in Lami Biological Reserve, southern Brazil

Fig. 1. Location of the study area in South America and the State of Rio Grande do Sul (left panel), with the indication of the geographic range of Leopardus guttulus (Hensel, 1872) (grey area) in Brazil, Paraguay and Argentina (above), and the Biological Reserve Lami JosÉ Lutzenberger – BRLJL in the municipality of Porto Alegre, Rio Grande do Sul, Brazil (below). On the right panel, a detailed map of the study area showing the limits of the BRLJL (black line), the vegetation types occurring in the area, the grid sQuares of 1 x 1 km (grey lines) designed to delimitate the zones where sampling stations (camera stations) were installed (black triangles).

Fig. 3 in Population structure and reproductive biology of Haemulopsis corvinaeformis (Perciformes, Haemulidae) in the south coast of Pernambuco, northeastern Brazil

Fig. 3. Monthly average (±SD) of the total length (TL, cm) of males, females and pooled sexes of Roughneck Grunt, Haemulopsis corvinaeformis (Steindachner, 1868), captured from August 2011 to July 2012, off the coast of state of Pernambuco, northeastern Brazil. Different letters indicate significant size differences between months for pooled sexes (∗, significant sizes differences between males and females; ∗∗, significant differences in sexual ratio).

Fig. 5 in Population structure and reproductive biology of Haemulopsis corvinaeformis (Perciformes, Haemulidae) in the south coast of Pernambuco, northeastern Brazil

Fig. 5. Total length at first sexual maturity (L 50, cm) and confidence interval (IC, 95%) for females, males and pooled sexes of Roughneck Grunt, Haemulopsis corvinaeformis (Steindachner, 1868), captured from August 2011 to June 2012, off the coast of state of Pernambuco, northeastern Brazil.

Fig. 4 in Aspects of biology of Megalobulimus paranaguensis (Gastropoda, Acavoidea) in the coastal plain of the Brazilian southeast

Fig. 4. Seasonal variation of temperature range per month in municipality of Santos during period sampled.

Fig. 3 in Aspects of biology of Megalobulimus paranaguensis (Gastropoda, Acavoidea) in the coastal plain of the Brazilian southeast

Fig. 3. Seasonal variation of mean temperature per month in municipality of Santos during period sampled.

Fig. 4 in Population structure and reproductive biology of Haemulopsis corvinaeformis (Perciformes, Haemulidae) in the south coast of Pernambuco, northeastern Brazil

Fig. 4. Bimonthly changes in GSI (± standard error) and frequency of the different gonadal stages for Roughneck Grunt, Haemulopsis corvinaeformis (Steindachner, 1868), captured from August 2011 to June 2012, off the coast of state of Pernambuco, northeastern Brazil (A, immature; B, maturing; C, mature; D, spawned or resting). The numbers above the line represent the sample size of GSI analysis in each bimester.

Fig. 2 in Aspects of biology of Megalobulimus paranaguensis (Gastropoda, Acavoidea) in the coastal plain of the Brazilian southeast

Fig. 2. Egg posture of Megalobulimus paranaguensis (Pilsbry & Ihering, 1900) in leaf litter (1b). Scale = 30 mm.

Fig. 1 in Aspects of biology of Megalobulimus paranaguensis (Gastropoda, Acavoidea) in the coastal plain of the Brazilian southeast

Fig. 1. Mean number of postures of Megalobulimus paranaguensis (Pilsbry & Ihering, 1900) in Parque Zoobotânico Orquidário Municipal de Santos (PZOMS).

Fig. 2 in Population structure and reproductive biology of Haemulopsis corvinaeformis (Perciformes, Haemulidae) in the south coast of Pernambuco, northeastern Brazil

Fig. 2. Absolute frequency distribution per length classes of males, females and pooled sexes for Roughneck Grunt, Haemulopsis corvinaeformis (Steindachner, 1868) captured from August 2011 to July 2014, off the coast of State of Pernambuco, northeastern Brazil. The vertical line represents the L50.

Fig. 1 in Population structure and reproductive biology of Haemulopsis corvinaeformis (Perciformes, Haemulidae) in the south coast of Pernambuco, northeastern Brazil

Fig. 1. Study area in the coast of state of Pernambuco, northeastern Brazil. Black dots represent fishing sites.

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Figure 1 in Advances in understanding bat infection dynamics across biological scales

Figure 1. Map illustrating the geographical and taxonomic diversity of bat species highlighted in case studies throughout the main text, with approximate study location and photo. Species names are coloured according to bat family, with a simplified phylogeny showing relationships between families. See electronic supplementary material for photo permissions.

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Figure 2 in Advances in understanding bat infection dynamics across biological scales

Figure 2. Overarching research priorities for future studies on bat infection dynamics, organized at the individual, population and community scales; S, susceptible; I, infected; R, recovered.

Fig. 8 in SYNOPSIS OF THE BIOLOGICAL DATA ON THE LOGGERHEAD SEA TURTLE CARETTA CARETTA (LINNAEUS 1758)

Fig. 8. Growth rates for loggerheads during the first year of activity. Figure from Frazer (1982). (%¼) Meanfrom Kaufmann (1967); (V) Mean from Caldwell et al. (1955); (•) Grand mean from Stickney et al. (1973);) (O) Mean from Rebel (1974); (%) Mean from Witham and Futch (1977).

Fig. 5 in SYNOPSIS OF THE BIOLOGICAL DATA ON THE LOGGERHEAD SEA TURTLE CARETTA CARETTA (LINNAEUS 1758)

Fig. 5. Worldwide nesting locations of the loggerhead. Stars represent major nesting locations arid circles indicate minor nesting areas.

Fig. 7 in SYNOPSIS OF THE BIOLOGICAL DATA ON THE LOGGERHEAD SEA TURTLE CARETTA CARETTA (LINNAEUS 1758)

Fig. 7. Histogram showing size frequency distribution of loggerheads stranded along European coasts of the Atlantic Ocean (Brongersma 1972).

Fig. 6 in SYNOPSIS OF THE BIOLOGICAL DATA ON THE LOGGERHEAD SEA TURTLE CARETTA CARETTA (LINNAEUS 1758)

Fig. 6. Nesting locations of the loggerhead in the west-central Atlantic Ocean and Caribbean Sea. Heavy stippling represents major areas of nesting; light stippling represents areas of lesser but still important nesting concentrations; arrows represent areas with sporadic but consistent nesting, or areas where loggerheads have nested only rarely.

Fig. 9 in SYNOPSIS OF THE BIOLOGICAL DATA ON THE LOGGERHEAD SEA TURTLE CARETTA CARETTA (LINNAEUS 1758)

Fig. 9. Growth rates for loggerheads beyond the first year in captivity. Figure from Frazer (1982). (%) Calculated from Uchida(1967); (O) Data for Parker's (1929) fastestgrowing turtle; (•) Mean for three other turtles of Parker's (1929); (V) Mean from Hildebrand and Hatsel (1927); (%¡) Mean from Hughes et al. (1967); (%¼) Grand mean from Schwartz (1981).

Fig. 3. A-C in SYNOPSIS OF THE BIOLOGICAL DATA ON THE LOGGERHEAD SEA TURTLE CARETTA CARETTA (LINNAEUS 1758)

Fig. 3. A-C Dorsal, ventral, and lateral views of skull of adult male loggerhead (100 cm CL) from Sanibel Island, FL (Pritchard and Trebbau 1984).