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FIGURE 5 in Pseudochromis lugubris and P. tonozukai, two new dottyback fish species from the Indo­Australian Archipelago (Perciformes: Pseudochromidae: Pseudochrominae)

FIGURE 5. Pseudochromis tonozukai, male, underwater photo, Weh Island, off northern Sumatra, Indonesia. (Photo by T. Tonozuka)

opencc-zeroDec 2004View details →
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FIGURE 1 in Pseudochromis lugubris and P. tonozukai, two new dottyback fish species from the Indo­Australian Archipelago (Perciformes: Pseudochromidae: Pseudochrominae)

FIGURE 1. Pseudochromis lugubris, underwater photo, Milne Bay, Papua New Guinea. (Photo by S. W. Michael)

opencc-zeroDec 2004View details →
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FIGURE 3 in Pseudochromis lugubris and P. tonozukai, two new dottyback fish species from the Indo­Australian Archipelago (Perciformes: Pseudochromidae: Pseudochrominae)

FIGURE 3. Pseudochromis bitaeniatus, underwater photo, Mabul, Sabah, Malaysia. (Photo by R. H. Kuiter).

opencc-zeroDec 2004View details →
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Fig.ç2.C olor variations of caudal ns of Upeneus guttatus from Kagoshima, Japan. A, KAUM–I. 7819, 57.8 mm SL; B, KAUM–I. 11885, 80.5 mm SL; C, KAUM–I. 24423, 84.3 mm SL; D, KAUM–I. 13067, 119.2 mm SL. in First Records of the Two-tone Goatfish, Upeneus guttatus, from Japan, and Comparisons with U. japonicus (Perciformes: Mullidae)

Fig.ç2.C olor variations of caudal ns of Upeneus guttatus from Kagoshima, Japan. A, KAUM–I. 7819, 57.8 mm SL; B, KAUM–I. 11885, 80.5 mm SL; C, KAUM–I. 24423, 84.3 mm SL; D, KAUM–I. 13067, 119.2 mm SL.

opencc-by-4.0May 2012View details →
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Fig.ç1.C olor photographs of fresh specimens of (A–B) Upeneus guttatus and (C–D) U. japonicus. A–B: KAUM–I. 11011, 114.1 mm SL, Kagoshima, Japan; C–D: KAUM–I. 9212, 90.9 mm SL, Kagoshima, Japan. in First Records of the Two-tone Goatfish, Upeneus guttatus, from Japan, and Comparisons with U. japonicus (Perciformes: Mullidae)

Fig.ç1.C olor photographs of fresh specimens of (A–B) Upeneus guttatus and (C–D) U. japonicus. A–B: KAUM–I. 11011, 114.1 mm SL, Kagoshima, Japan; C–D: KAUM–I. 9212, 90.9 mm SL, Kagoshima, Japan.

opencc-by-4.0May 2012View details →
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Fig.ç3.R elationships of (A) barbel length and (B) pectoral- n length to standard length in Upeneus guttatus (closed symbols: stars from Japan, squares from Indo–West Paci c) and U. japonicus (open circles). in First Records of the Two-tone Goatfish, Upeneus guttatus, from Japan, and Comparisons with U. japonicus (Perciformes: Mullidae)

Fig.ç3.R elationships of (A) barbel length and (B) pectoral- n length to standard length in Upeneus guttatus (closed symbols: stars from Japan, squares from Indo–West Paci c) and U. japonicus (open circles).

opencc-by-4.0May 2012View details →
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Figure 2 in Review of the family Serranidae (Perciformes) from the Canary Islands (eastern-central Atlantic), with the first records of Serranus hepatus and Epinephelus aeneus

Figure 2. – Serranus hepatus from Tenerife, Canary Islands (GBIF-CFM-IEOCA 1199, 86.0 mm TL, 69.2 mm SL) (Credits: J.F. González-Jiménez, 2020).

opencc-by-4.0Dec 2021View details →
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Figure 1 in Review of the family Serranidae (Perciformes) from the Canary Islands (eastern-central Atlantic), with the first records of Serranus hepatus and Epinephelus aeneus

Figure 1. – The Canary Islands. Collection and sighting locations: (Ê) Serranus hepatus; (■) Epinephelus aeneus; (●) Epinephelus costae (map adapted from BlueChart Atlantic v9.5).

opencc-by-4.0Dec 2021View details →
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Fig. 5. Mean Gonadosomatic Index for C in Color pattern variation in Cichla temensis (Perciformes: Cichlidae): Resolution based on morphological, molecular, and reproductive data

Fig. 5. Mean Gonadosomatic Index for C. temensis variants grouped by CPV grade. a) Females from the Igapó Açú (Region 1). b) Females from the rio Caures (Region 2). c) Males from the Igapó Açú region. d) Males from the rio Caures. A significant correlation between GSI and CPV Grade was found for males and females in both collecting regions, p <.01 for a, b, d, and d.

opencc-by-4.0Dec 2012View details →
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Fig. 4 in Color pattern variation in Cichla temensis (Perciformes: Cichlidae): Resolution based on morphological, molecular, and reproductive data

Fig. 4. Maximum-likelihood phylogeny of 50 sequences sampled from the paca and açu variants of Cichla temensis (Genbank accession numbers HQ230011 - HQ230016) The phylogeny was rooted a posteriori with Cichla species of the clade A (sensu Willis et al. 2010) (GU295691- GU295704). The scale represents an HKY85 genetic distance.

opencc-by-4.0Dec 2012View details →
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Fig. 3. a in Color pattern variation in Cichla temensis (Perciformes: Cichlidae): Resolution based on morphological, molecular, and reproductive data

Fig. 3. a) Mean (± SEM) lateral line scale counts for C. temensis, C. monoculus, and C. orinocensis. ANOVA showed no significant differences among the C. temensis variants but revealed significant differences interspecifically. Post hoc t tests (horizontal starred bar) revealed that all species were significantly different, p <0.0001*. b) Mean (± SEM) body depth to Standard Length ratio (adjusted for gonad size differential) for C. temensis, C. monoculus, and C. orinocensis. ANOVA showed no significant differences among the C. temensis variants but revealed significant differences interspecifically. Post hoc t tests (horizontal starred bar) revealed that all C. temensis were significantly different from both sympatric species, p <0.0001*.

opencc-by-4.0Dec 2012View details →
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Fig. 2 in Color pattern variation in Cichla temensis (Perciformes: Cichlidae): Resolution based on morphological, molecular, and reproductive data

Fig. 2. Collecting regions in two cyclically flooding drainages in the rio Amazon basin. Region 1, the Igapó-Açu region, a blackwater tributary complex of the rio Madeira, provided specimens of C. temensis and C. monoculus. Region 2, the rio Caures, a blackwater tributary of the rio Negro, provided specimens of C. temensis and C. orinocensis.

opencc-by-4.0Dec 2012View details →
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Fig. 3 in Distributional Range Extension of the Shallow Water Scorpionfish Parascorpaena poseidon (Perciformes: Scorpaenidae), with a Revised Diagnosis of the Species

Fig. 3. Lateral (A) and dorsal (B) views of head of Parascorpaena poseidon (NSMT-P 17865, 97.8 mm SL). Bars indicate 5 mm.

opencc-by-4.0Apr 2024View details →
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Fig. 4 in Distributional Range Extension of the Shallow Water Scorpionfish Parascorpaena poseidon (Perciformes: Scorpaenidae), with a Revised Diagnosis of the Species

Fig. 4. Relationships between body width (A); head width (B); snout length (C); interorbital width at vertical midline of eye (D); upper-jaw length (E); maxilla depth (F); postorbital length (G); orbit diameter (H); and separation between opercular spine tips (I) (all as % of SL) and standard length (mm) in Parascorpaena poseidon, showing ontogenetic changes. Star indicates holotype [except for snout length, interorbital width at vertical midline of eye, and upper-jaw length—see text regarding measurements by Chou and Liao (2022)].

opencc-by-4.0Apr 2024View details →
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Fig. 2 in Distributional Range Extension of the Shallow Water Scorpionfish Parascorpaena poseidon (Perciformes: Scorpaenidae), with a Revised Diagnosis of the Species

Fig. 2. Variously-sized preserved specimens of Parascorpaena poseidon. A, FMNH 75818, 1 of 27 specimens, 35.3 mm SL, Galle, Sri Lanka; B, FMNH 75818, 1 of 27 specimens, 65.3 mm SL, Galle, Sri Lanka; C, NSMT-P 17865, 97.8 mm SL, Yaku-shima Island, Osumi Islands, Kagoshima, Japan; D, BPBM 27680, 1 of 2 specimens, 115.4 mm SL, Kovalam, Kerala India.

opencc-by-4.0Apr 2024View details →
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Fig. 1 in Distributional Range Extension of the Shallow Water Scorpionfish Parascorpaena poseidon (Perciformes: Scorpaenidae), with a Revised Diagnosis of the Species

Fig. 1. Fresh specimen of Parascorpaena poseidon from Kovalam, Kerala, India (BPBM 27680, 1 of 2 specimens, 115.4 mm SL). Photo by J. E. Randall (BPBM).

opencc-by-4.0Apr 2024View details →
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Fig. 5 in Distributional Range Extension of the Shallow Water Scorpionfish Parascorpaena poseidon (Perciformes: Scorpaenidae), with a Revised Diagnosis of the Species

Fig. 5. Distributional records of Parascorpaena poseidon, based on original description (triangles and star), literature record as P. mossambica (closed circle), and present study (open circles). Star indicates type locality.

opencc-by-4.0Apr 2024View details →
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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).

opencc-by-4.0Jun 2018View details →
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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.

opencc-by-4.0Jun 2018View details →
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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.

opencc-by-4.0Jun 2018View details →

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International Brain Laboratory public data

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