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54 results for “Nephropidae”
FIGURE 2 in Distribution of two species of Nephropsis Wood-Mason, 1872 (Crustacea, Decapoda, Nephropidae) from northeastern Brazil
FIGURE 2. Geographic distribution of Nephropsis agassizii A. Milne-Edwards, 1880 and Nephropsis neglecta Holthuis, 1974 in the Atlantic Ocean. Black symbols = previous records; gray symbols = new records.
FIGURE 1. Nephropsis agassizii A in Distribution of two species of Nephropsis Wood-Mason, 1872 (Crustacea, Decapoda, Nephropidae) from northeastern Brazil
FIGURE 1. Nephropsis agassizii A. Milne-Edwards, 1880, female, TL 103 mm, Bpot-Talude MT-83, MOUFPE 15.152. A, dorsal habitus; B, carapace, dorsal view; C, abdomen, right lateral view. Scale bar = 1 cm.
FIGURE 3. Nephropsis neglecta Holthuis, 1974 in Distribution of two species of Nephropsis Wood-Mason, 1872 (Crustacea, Decapoda, Nephropidae) from northeastern Brazil
FIGURE 3. Nephropsis neglecta Holthuis, 1974, ovigerous female, TL 84 mm, Bpot-Talude MT 71-2, MOUFPE 15.153. A, dorsal habitus; B, carapace, dorsal view; C, abdomen, right lateral view. Scale bar = 1 cm.
FIGURE 5. Families Scyllaridae and Nephropidae. A in Checklist of decapod crustaceans from the coast of the São Paulo state (Brazil) supported by integrative molecular and morphological data: V. Dendrobranchiata and Pleocyemata [Achelata, Astacidea, Axiidea, Caridea (Alpheoidea and Processoidea excluded), Gebiidea, Stenopodidea]
FIGURE 5. Families Scyllaridae and Nephropidae. A) Scyllarides deceptor Holthuis, 1963 (CCDB 5280). B) Scyllarus depressus (Smith, 1881) (CCDB 5775). C) Metanephrops rubellus (Moreira, 1903) (CCDB 5796). Animals from Brazil, São Paulo, Ubatuba (A), R/V Soloncy Moura Expedition, st. 8 (B), st. 14 (C). Sex: male (A, C), female (B). Scale bars (mm): A—23; B—18; C—40. Photographs by R.C. Buranelli.
FIGURE 4 in A new species of Pseudione Kossmann, 1881 (Isopoda, Cymothoida, Bopyridae) parasitizing the lobster Nephropsis aculeata Smith, 1881 (Decapoda, Astacidea, Nephropidae) in the Southwestern Atlantic
FIGURE 4. Distribution of the species of Pseudione Kossmann, 1881 that parasite Nephropidae lobsters.
FIGURE 2 in A new species of Pseudione Kossmann, 1881 (Isopoda, Cymothoida, Bopyridae) parasitizing the lobster Nephropsis aculeata Smith, 1881 (Decapoda, Astacidea, Nephropidae) in the Southwestern Atlantic
FIGURE 2. Pseudione ivanklini sp. nov., female holotype and paratype: A, habitus dorsal view (MZUSP 38163); B, habitus ventral view (MZUSP 38163); C, antennula (MZUSP 38163); D, antenna (MZUSP 38163); E, barbula left side (MZUSP 38163); F, maxilliped, outer view (paratype, MZUSP 38165); G, maxilliped palp (MZUSP 38165); H, maxilliped spur (MZUSP 38165); I, oostegite 1, outer view (MZUSP 38163); J, oostegite 1, inner view (MZUSP 38163); K, left pereopod 1 (MZUSP 38163); L, left pereopod 7 (MZUSP 38163). Scale bars: A and B = 3.33 mm; C = 0.25mm; D and G = 0.5 mm; E = 0.1 mm; F, K and L = 1.00 mm; H = 0.3 mm; I and J = 1.5 mm.
FIGURE 1 in A new species of Pseudione Kossmann, 1881 (Isopoda, Cymothoida, Bopyridae) parasitizing the lobster Nephropsis aculeata Smith, 1881 (Decapoda, Astacidea, Nephropidae) in the Southwestern Atlantic
FIGURE 1. Pseudione ivanklini sp. nov., host, holotype and male paratype: A, host Nephropsis aculeata (Smith, 1881) with the parasites in the right branchial chamber (UFRGS 6584); B, mature female ventral view (holotype, MZUSP 38163) bearing a dwarf male in the pleon; C, dwarf male dorsal view (paratype, MZUSP 38164). Abbreviations: p = parasites; ma = marsupium; dm = dwarf male. Scale bars: A = 2.5 cm; B = 3.3 mm and C = 1.5 mm.
FIGURE 3 in A new species of Pseudione Kossmann, 1881 (Isopoda, Cymothoida, Bopyridae) parasitizing the lobster Nephropsis aculeata Smith, 1881 (Decapoda, Astacidea, Nephropidae) in the Southwestern Atlantic
FIGURE 3. Pseudione ivanklini sp. nov., male paratype (MZUSP 38164): A, habitus ventral view; B, habitus dorsal view; C, antennula; D, antenna; E, left pereopod 1; F, left pereopod 7. Scale bars: A and B = 1.5 mm; C and D = 0.1 mm; E and F = 0.25 mm.
Figure 10 in Distribution and reproductive biology of a subantarctic deep-sea lobster, the Patagonian lobsterette Thymops birsteini (Zarenkov and Semenov, 1972) (Decapoda, Astacidea, Nephropidae)
Figure 10. Egg numbers on female pleiopods and equation showing the relationship between egg number at Stage 1 and female carapace length.
Figure 6 in Distribution and reproductive biology of a subantarctic deep-sea lobster, the Patagonian lobsterette Thymops birsteini (Zarenkov and Semenov, 1972) (Decapoda, Astacidea, Nephropidae)
Figure 6. Changes in the sex ratio with depth (samples comprising fewer than 100 animals are indicated by small dots).
Figure 1 in Distribution and reproductive biology of a subantarctic deep-sea lobster, the Patagonian lobsterette Thymops birsteini (Zarenkov and Semenov, 1972) (Decapoda, Astacidea, Nephropidae)
Figure 1. Distribution of Thymops birsteini in the southwest Atlantic: stations where the species was recorded (A) and position from which samples were collected (B). Black dots indicate catches of trawlers; grey dots indicate catches of potters.
Figure 2 in Distribution and reproductive biology of a subantarctic deep-sea lobster, the Patagonian lobsterette Thymops birsteini (Zarenkov and Semenov, 1972) (Decapoda, Astacidea, Nephropidae)
Figure 2. Changes in vessel catches per unit effort (CPUE) with depth. Confidence intervals (a50.05) are shown by error bars.
Figure 9 in Distribution and reproductive biology of a subantarctic deep-sea lobster, the Patagonian lobsterette Thymops birsteini (Zarenkov and Semenov, 1972) (Decapoda, Astacidea, Nephropidae)
Figure 9. Individual larvae (A, B) and their attachment to female pleiopods (C, D). Scale bar is 1 mm.
Figure 3 in Distribution and reproductive biology of a subantarctic deep-sea lobster, the Patagonian lobsterette Thymops birsteini (Zarenkov and Semenov, 1972) (Decapoda, Astacidea, Nephropidae)
Figure 3. Changes in length – frequency distributions of Thymops birsteini with depth in catches of trawlers (A) and potters (B).
Figure 7 in Distribution and reproductive biology of a subantarctic deep-sea lobster, the Patagonian lobsterette Thymops birsteini (Zarenkov and Semenov, 1972) (Decapoda, Astacidea, Nephropidae)
Figure 7. Changes in occurrence of the different maturity stages with female size (A) and with season (B). Only females larger than 40 mm carapace length were included in (B).
FIGURE 1 in Validation of Metanephrops serendipitus (Crustacea, Decapoda, Nephropidae), a deep-water lobster from lower Miocene of Meljski hrib (Maribor, Slovenia)
FIGURE 1. Metanephrops serendipitus sp. nov., holotype specimen RGA/SMNH 2295 (carapace) and RGA/SMNH 1591 (chelipeds). Scale bar equals 10 mm.
Figure 2 from: Chang S-C, Chan T-Y, Kumar AB (2020) Deep-sea clawed lobster Nephropsis stewarti Wood-Mason, 1872 species complex in the Indo-West Pacific (Crustacea, Decapoda, Nephropidae), with description of a new species. ZooKeys 1008: 37-60. https://doi.org/10.3897/zookeys.1008.59966
Figure 2 Nephropsis grandis Zarenkov, 2006, Tanimbar Islands, Arafura Sea, KARUBAR stn CP59, neotype male cl 64.1 mm (MNHN IU-2017-9001) A carapace and pleon, dorsal B same, lateral C left pereiopod I, chela to distal part of merus, dorsal D same, lateral E same, ventral. Pubescence and setae omitted ● Position of spines on inner surface of palm ◇ position of spines on dorsal margin of outer surface ♦ position of spines on dorsal margin of inner surface ⏹ dorso-inner distal spine of carpus △ ventro-outer distal spine of carpus ◻ distoventral spine ✰ subdistal dorsal spine of merus ★ position of subdistal outer spine of merus.
Figure 1 from: Chang S-C, Chan T-Y, Kumar AB (2020) Deep-sea clawed lobster Nephropsis stewarti Wood-Mason, 1872 species complex in the Indo-West Pacific (Crustacea, Decapoda, Nephropidae), with description of a new species. ZooKeys 1008: 37-60. https://doi.org/10.3897/zookeys.1008.59966
Figure 1 Nephropsis stewarti Wood-Mason, 1872, Andaman Sea, RV 'Dr. Fridtjof Nansen' stn 135, neotype male cl 46.2 mm (NTOU M02249) A carapace and pleon, dorsal B same, lateral C left pereiopod I, chela to distal part of merus, dorsal D same, lateral E same, ventral. Pubescence and setae omitted ● Position of spines on inner surface of palm ◇ position of spines on dorsal margin of outer surface of carpus ♦ position of spines on dorsal margin of inner surface of carpus ⏹ dorso-inner distal spine of carpus △ ventro-outer distal spine of carpus ◻ distoventral spine ✰ subdistal dorsal spine of merus ★ position of subdistal outer spine of merus.
Figure 5 from: Chang S-C, Chan T-Y, Kumar AB (2020) Deep-sea clawed lobster Nephropsis stewarti Wood-Mason, 1872 species complex in the Indo-West Pacific (Crustacea, Decapoda, Nephropidae), with description of a new species. ZooKeys 1008: 37-60. https://doi.org/10.3897/zookeys.1008.59966
Figure 5 A, BN. grandis Zarenkov, 2006, Dasi fishing port, Taiwan, male cl 45.3 mm (NTOU M02171) C, DN. pygmaea sp. nov., Donggang fishing port, Taiwan, paratype female cl 24.4 mm (NTOU M02168) A, C dorsal habitus B, D lateral habitus.
Figure 4 from: Chang S-C, Chan T-Y, Kumar AB (2020) Deep-sea clawed lobster Nephropsis stewarti Wood-Mason, 1872 species complex in the Indo-West Pacific (Crustacea, Decapoda, Nephropidae), with description of a new species. ZooKeys 1008: 37-60. https://doi.org/10.3897/zookeys.1008.59966
Figure 4 A–FNephropsis stewarti Wood-Mason, 1872 A, B Sakthikulangara fishing harbor, India, ovigerous female cl 42.4 mm (DABFUK/AR-ACH-10) C, D Mozambique, MAINBAZA stn CP3138, male cl 52.7 mm (MNHN IU-2018-5063) E Andaman Sea, RV 'Dr. Fridtjof Nansen' stn 135, neotype male cl 46.2 mm (NTOU M02249) F Andaman Sea, RV 'Dr. Fridtjof Nansen' stn 68, male cl 42.3 mm (NTOU M02250) A, C, E, F dorsal habitus B, D lateral habitus E, F photographed by PN Psomadakis.
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