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96 results for “Engraulidae”
Fig. 2 in Morphological development of Anchoviella vaillanti (Steindachner, 1908) (Clupeiformes: Engraulidae) larvae and early juveniles
Fig. 2. Variation of (a) predorsal (PDL) and (b) preanal (PAL) lengths as percentage of standard length (SL) of larvae and juveniles of Anchoviella vaillanti, and (c) mean values for PDL/SL and PAL/SL for larval stages (preflexion, flexion and postflexion) and juveniles. Mean values; box: mean±standard deviation, whisker: minimum-maximum values.
Fig. 3 in Habitat selection by anchovies (Clupeiformes: Engraulidae) in a tropical bay at Southeastern Brazil
Fig. 3. Canonical correspondence analysis ordination diagram of juvenile Engraulidae abundance data, with environmental variables. Bay Zones: Sites 1, 2 and 3 (outer); 4 and 5 (inner).
Fig. 4 in Habitat selection by anchovies (Clupeiformes: Engraulidae) in a tropical bay at Southeastern Brazil
Fig. 4. Canonical correspondence analysis ordination diagram of adults Engraulidae abundance data, with environmental variables. Samples coded by seasons.
Fig. 2 in Habitat selection by anchovies (Clupeiformes: Engraulidae) in a tropical bay at Southeastern Brazil
Fig. 2. Spatial and seasonal densities of juveniles A. januaria (o) and A. tricolor (l) in the Sepetiba Bay, 1998/2000. Each sample (mark in the graphic) represents the total number of fish.
Fig. 1 in Habitat selection by anchovies (Clupeiformes: Engraulidae) in a tropical bay at Southeastern Brazil
Fig. 1. Study area, Sepetiba Bay, Brazil, with indication of the beach seine sampling sites (1-5). a - rio Prata; b - rio Corumbi; c - rio Cação; d - rio Mazomba; e - rio Guarda; f - canal São Francisco; g - canal Guandu; h - canal Itá; i - rio Piraquê; j - rio Piracão.
Fig. 11 in Resurrection of nominal species previously regarded as junior synonyms of Thrissina baelama (Fabricius, 1775) and their re-descriptions (Teleostei: Clupeiformes: Engraulidae)
Fig. 11. Dorsal fins of A, Thrissina tuberculosa (BPBM 20277, 86.6 mm SL, Mauritius; triangles indicate several distinct dark spots scattered on anterior part), B, T. baelama (BMNH 1963.12.9.1–19, 102.4 mm SL, Djibouti), C, T. evermanni [BPBM 41796, 87.3 mm SL, Tonga (left-right inverted)], D, T. polynemoides (BMNH 1966.11.16.985–992, 89.5 mm SL, Mombasa, Kenya), and E, T. samam (BMNH 1971.2.8.50–58, 75.3 mm SL, New Britain, Papua New Guinea).
Fig. 10 in Resurrection of nominal species previously regarded as junior synonyms of Thrissina baelama (Fabricius, 1775) and their re-descriptions (Teleostei: Clupeiformes: Engraulidae)
Fig. 10. Neotype of Clupea tuberculosa, BPBM 41797, 90.9 mm SL, Black River District, Mauritius (also neotype of Engraulis nesogallicus): A, fresh condition (courtesy of Bishop Museum); B, preserved condition.
Fig. 8. A in Resurrection of nominal species previously regarded as junior synonyms of Thrissina baelama (Fabricius, 1775) and their re-descriptions (Teleostei: Clupeiformes: Engraulidae)
Fig. 8. A, Holotype of Engraulis polynemoides (BMNH 1979.7.5.26, 93.3 mm SL, Madagascar), and B, non-type specimen of T. polynemoides (BMNH 1966.11.16.985–992, 94.0 mm SL, Mombasa, Kenya).
Fig. 9. A in Resurrection of nominal species previously regarded as junior synonyms of Thrissina baelama (Fabricius, 1775) and their re-descriptions (Teleostei: Clupeiformes: Engraulidae)
Fig. 9. A, Neotype of Engraulis samam (BMNH 1971.2.8.49, 79.6 mm SL, New Britain, Papua New Guinea), and B, non-type specimen of Thrissina samam (fresh condition) (NSMT-P 145681, 87.4 mm SL, Sulawesi, Indonesia).
Fig. 7 in Resurrection of nominal species previously regarded as junior synonyms of Thrissina baelama (Fabricius, 1775) and their re-descriptions (Teleostei: Clupeiformes: Engraulidae)
Fig. 7. Morphometrics of Thrissina baelama (blue triangles ▲), T. evermanni (yellow squares ■), T. polynemoides (green diamonds ◆), T. samam (red circles ●), and T. tuberculosa (pink stars) (all vs. standard length; SL). A, Ratio of caudal-peduncle depth to SL; B, pre-dorsal-fin length to SL; C, snout length to SL, D, body depth to SL; E, pre-anal-fin length to SL; F, dorsal-fin base length to SL; G, distance from pelvic-fin insertion to anal-fin origin to SL; H, pectoral-fin length to SL; I, pelvic-fin length to SL; J, maxilla length to SL; K, lower-jaw length to SL; L, caudal-peduncle length to SL.
Fig. 6 in Resurrection of nominal species previously regarded as junior synonyms of Thrissina baelama (Fabricius, 1775) and their re-descriptions (Teleostei: Clupeiformes: Engraulidae)
Fig. 6. Relationships of total gill-raker numbers (TGR) on A, first gill arch (1GA), B, second gill arch (2GA), C, third gill arch (3GA), and D, fourth gill arch (4GA) to standard length in Thrissina baelama (blue triangles ▲), T. evermanni (yellow squares ■), T. polynemoides (green diamonds ◆), T. samam (red circles ●), and T. tuberculosa (pink stars).
Fig. 1. A–D in Resurrection of nominal species previously regarded as junior synonyms of Thrissina baelama (Fabricius, 1775) and their re-descriptions (Teleostei: Clupeiformes: Engraulidae)
Fig. 1. A–D, Diagnostic characters of species previously identified as Thrissina baelama [A, lateral view of whole body, B, head (yellow line indicates posterior part of maxilla; blue line and broken lines indicate anterior and posterior margins of preopercle, respectively), C, first and second supramaxillae (left-right inverted), D, ventral view of isthmus (no scutes located anterior to pectoral fins)] and E, ventral view of isthmus of Thrissina encrasicholoides (scutes located anterior to pectoral fins) (A: fresh condition, 72.9 mm SL, Sulawesi, Indonesia; B–D: T. samam, NSMT-P 144842, 58.4 mm SL, Ryukyu Archipelago, Japan; E: T. encrasicholoides, NSMT-P 50306, 69.8 mm SL, Philippines) (B–E, alizarin stain).
Fig. 3. A in Resurrection of nominal species previously regarded as junior synonyms of Thrissina baelama (Fabricius, 1775) and their re-descriptions (Teleostei: Clupeiformes: Engraulidae)
Fig. 3. A, Neotype of Clupea baelama, BMNH 1963.12.9.27, 69.5 mm SL, Red Sea near Port Sudan, Sudan, and B, non-type specimen of Thrissina baelama (fresh condition) (BPBM 27411, 83.4 mm SL, Port Sudan, Sudan; courtesy of Bishop Museum).
Fig. 5. A in Resurrection of nominal species previously regarded as junior synonyms of Thrissina baelama (Fabricius, 1775) and their re-descriptions (Teleostei: Clupeiformes: Engraulidae)
Fig. 5. A, Holotype of Anchovia evermanni, USNM 51719, 105.0 mm, and B, paratype of Anchovia evermanni, USNM 451580, 98.3 mm SL, Apia, Samoa.
Fig. 4 in Resurrection of nominal species previously regarded as junior synonyms of Thrissina baelama (Fabricius, 1775) and their re-descriptions (Teleostei: Clupeiformes: Engraulidae)
Fig. 4. Distributional records of Thrissina baelama (triangles), T. evermanni (squares), T. polynemoides (diamonds), T. samam (circles), and T. tuberculosa (star), based on specimens examined in this study.
Fig. 2 in Resurrection of nominal species previously regarded as junior synonyms of Thrissina baelama (Fabricius, 1775) and their re-descriptions (Teleostei: Clupeiformes: Engraulidae)
Fig. 2. Scatter plots of principal component 2 and 3 scores on 26 measurements and counts of total gill rakers on first to fourth gill arches for specimens of Thrissina baelama (triangles), T. evermanni (squares), T. polynemoides (diamonds), T. samam (circles), and T. tuberculosa (stars).
Fig. 1 in The Relationship Between Fish Length And Otolith Size And Weight Of The Australian Anchovy, Engraulis Australis (Clupeiformes, Engraulidae), Retrieved From The Food Of The Australasian Gannet, Morus Serrator (Suliformes, Sulidae), Hauraki Gulf, New Zealand
Fig. 1. Map showing the location of the gannet's colonies in
FIGURE 5 in Integrative systematics unveils the controversial identity of Engraulidae fishing stocks in a Neotropical estuary, northeast Brazil
FIGURE 5 | Canonical Variables Analysis discriminating for six pilombetas species.
Fig. 2 in Reproductive studies of Anchoa marinii Hildebrand, 1943 (Actinopterygii: Engraulidae) in the nearby-coastal area of Mar Chiquita coastal lagoon, Buenos Aires, Argentina
Fig. 2. Monthly relative frequency (%) of gonad phases for females of Anchoa marinii.
Fig. 5 in Reproductive studies of Anchoa marinii Hildebrand, 1943 (Actinopterygii: Engraulidae) in the nearby-coastal area of Mar Chiquita coastal lagoon, Buenos Aires, Argentina
Fig. 5. Oocyte diameter distribution in spawning capable phase of Anchoa marinii. N= 183.
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