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122 results for “Pandalidae”
Figure 8 in Unraveling distributional patterns and life-history traits of a deep-water shrimp Plesionika edwardsii (Decapoda, Pandalidae) under unexploited virgin conditions: a benchmark for fisheries management
Figure 8. Hypothesized life cycle of Plesionika edwardsii in the Azorean region. After the incubation period of shrimp eggs, (1) larvae are released into the water column and (2) juveniles develop in shallow waters. Mature females and males are distributed up to 600 m with a sexual segregation by depth: (3) non-ovigerous females are mainly found up to 200 m, (4) ovigerous females between 200 and 300 m, and (5) males from 400 to 500 m deep. Females are bigger than males, and ovigerous females are bigger than nonovigerous females. A bigger-deeper trend is observed up to 400 m. (6) Long larval stages of P. edwardsii increases its potential for dispersal (Landeira et al., 2009), favoring connectivity and stock homogeneity between adjacent areas.
Figure 5 in Unraveling distributional patterns and life-history traits of a deep-water shrimp Plesionika edwardsii (Decapoda, Pandalidae) under unexploited virgin conditions: a benchmark for fisheries management
Figure 5. Sex ratio of Plesionika edwardsii by depth stratum in the Azorean region during the period 1999–2000.
Figure 2 in Unraveling distributional patterns and life-history traits of a deep-water shrimp Plesionika edwardsii (Decapoda, Pandalidae) under unexploited virgin conditions: a benchmark for fisheries management
Figure 2. Seasonal predicted mean catch per unit effort (CPUE, g trap-1) by depth stratum for males, non-ovigerous and ovigerous females of Plesionika edwardsii in the Azorean region for the period 1999–2000. Light-colored symbols represent raw data. Detailed parameter estimates are in Tab. S4.
Figure 7 in Unraveling distributional patterns and life-history traits of a deep-water shrimp Plesionika edwardsii (Decapoda, Pandalidae) under unexploited virgin conditions: a benchmark for fisheries management
Figure 7. Size at which 50 % of the shrimps are mature (L 50) estimated for Plesionika edwardsii in the Azorean region fitting a logistic curve to the proportion of ovigerous females. Logistic curve was estimated combining all data obtained during the period 1999–2000.
Figure 4 in Unraveling distributional patterns and life-history traits of a deep-water shrimp Plesionika edwardsii (Decapoda, Pandalidae) under unexploited virgin conditions: a benchmark for fisheries management
Figure 4. Seasonal predicted mean cephalothorax length (CL) by depth stratum for males, non-ovigerous and ovigerous females of Plesionika edwardsii in the Azorean region for the period 1999–2000. Light-colored symbols represent raw data. Detailed parameter estimates are in Tab. S4.
Figure 1 in Unraveling distributional patterns and life-history traits of a deep-water shrimp Plesionika edwardsii (Decapoda, Pandalidae) under unexploited virgin conditions: a benchmark for fisheries management
Figure 1. Sampling areas of Plesionika edwardsii in the mid-North Atlantic Ocean, Azorean region (ICES Subdivision 10a2) between 1999 and 2000. Orange dots represent each site sampled by a trap.
Figure 6 in Unraveling distributional patterns and life-history traits of a deep-water shrimp Plesionika edwardsii (Decapoda, Pandalidae) under unexploited virgin conditions: a benchmark for fisheries management
Figure 6. Sex ratio of Plesionika edwardsii by size class in the Azorean region during the period 1999–2000.
Figure 3 in Unraveling distributional patterns and life-history traits of a deep-water shrimp Plesionika edwardsii (Decapoda, Pandalidae) under unexploited virgin conditions: a benchmark for fisheries management
Figure 3. Size frequency distribution of males, non-ovigerous and ovigerous females Plesionika edwardsii in the Azorean region during the period 1999-2000.
Figure 6. Pandalus gracilis Stimpson, stage 5 in Larval development of Pandalus gracilis Stimpson (Crustacea: Decapoda: Pandalidae) reared in the laboratory
Figure 6. Pandalus gracilis Stimpson, stage 5. (A) Dorsal view (scale bar: ab); (B) lateral view (ab); (C) antennule (ad); (D) antenna (ad); (E) mandibles (ae); (F) maxillule (ae); (G) maxilla (ae); (H) first maxilliped (ae); (I) second maxilliped (ae); (J) third maxilliped (ad); (K–O) left pereiopods 1–5 (ac); (P–T) pleopods 1–5 (ae); (U) telson (ac). Scale bars: 2 mm.
Figure 2. Pandalus gracilis Stimpson, stage 1 in Larval development of Pandalus gracilis Stimpson (Crustacea: Decapoda: Pandalidae) reared in the laboratory
Figure 2. Pandalus gracilis Stimpson, stage 1. (A) Dorsal view (scale bar: ab); (B) lateral view (ab); (C) antennule (ad); (D) antenna (ad); (E) mandibles (ae); (F) maxillule (ae); (G) maxilla (ae); (H) first maxilliped (ae); (I) second maxilliped (ae); (J) third maxilliped (ad); (K) right pereiopod 2 (ac); (L–P) left pereiopods 1–5 (ac); (Q) telson (ac). Scale bars: 1 mm.
Figure 1 in Larval development of Pandalus gracilis Stimpson (Crustacea: Decapoda: Pandalidae) reared in the laboratory
Figure 1. Pandalus gracilis Stimpson. Survival and duration of larval stages reared under laboratory conditions of 15°C and 33.7‰.
Figure 4. Pandalus gracilis Stimpson, stage 3 in Larval development of Pandalus gracilis Stimpson (Crustacea: Decapoda: Pandalidae) reared in the laboratory
Figure 4. Pandalus gracilis Stimpson, stage 3. (A) Dorsal view (scale bar: ab); (B) lateral view (ab); (C) antennule (ad); (D) antenna (ad); (E) mandibles (ae); (F) maxillule (ae); (G) maxilla (ae); (H) first maxilliped (ae); (I) second maxilliped (ae); (J) third maxilliped (ad); (K–O) left pereiopods 1–5 (ac); (P–T) pleopods 1–5 (ae); (U) telson (ac). Scale bars: 2 mm.
Figure 5. Pandalus gracilis Stimpson, stage 4 in Larval development of Pandalus gracilis Stimpson (Crustacea: Decapoda: Pandalidae) reared in the laboratory
Figure 5. Pandalus gracilis Stimpson, stage 4. (A) Dorsal view (scale bar: ab); (B) lateral view (ab); (C) antennule (ad); (D) antenna (ad); (E) mandibles (ae); (F) maxillule (ae); (G) maxilla (ac); (H) first maxilliped (ae); (I) second maxilliped (ae); (J) third maxilliped (ad); (K–O) left pereiopods 1–5 (ac); (P–T) pleopods 1–5 (ae); (U) telson (ac). Scale bars: 2 mm.
Figure 3. Pandalus gracilis Stimpson, stage 2 in Larval development of Pandalus gracilis Stimpson (Crustacea: Decapoda: Pandalidae) reared in the laboratory
Figure 3. Pandalus gracilis Stimpson, stage 2. (A) Dorsal view (scale bar: ab); (B) lateral view (ab); (C) antennule (ac); (D) antenna (ac); (E) mandibles (ad); (F) maxillule (ad); (G) maxilla (ad); (H) first maxilliped (ad); (I) second maxilliped (ad); (J) third maxilliped (ac); (K–O) left pereiopods 1–5 (ac); (P) telson (ac). Scale bars: 1 mm.
FIGURE 6 in Report on some Plesionika Bate, 1888 and first record of Stylopandalus Coutiére, 1905 (Caridea, Pandalidae) from Brazilian waters
FIGURE 6. Plesionika miles (A. Mine Edwards, 1883), ovigerous female, MNRJ 14661 (carapace length 11.4mm); A, propod and dactyl of pereopod 3, lateral view; B, dactyl of pereopod 3, lateral view. P. m i l e s (A. Mine Edwards, 1883), ovigerous female, MNRJ 14661 (carapace length 9mm); C, pleura of abdominal somites 3–5, lateral view (AS, abdominal somite). P. miles (A. Mine Edwards, 1883), male, MNRJ 14661 (carapace length 9mm); D, telson and uropods, dorsal view.
FIGURE 3 in Report on some Plesionika Bate, 1888 and first record of Stylopandalus Coutiére, 1905 (Caridea, Pandalidae) from Brazilian waters
FIGURE 3. Plesionika ensis (A. Milne Edwards, 1881), male, MNRJ 14658 (carapace length 15mm); A, lateral view; B, right antennule, dorsal view; C, right scaphocerite, dorsal view (as, antennal spine; ps, pterygostomian spine; st, stylocerite); D, right pereopod 2, dorsal view; E, left pereopod 2, dorsal view.
FIGURE 2 in Report on some Plesionika Bate, 1888 and first record of Stylopandalus Coutiére, 1905 (Caridea, Pandalidae) from Brazilian waters
FIGURE 2. Plesionika edwardsii (Brandt, 1851), female, MNRJ 14655 (carapace length 21.5mm); A, propod and dactyl of pereopod 3, lateral view; B, dactyl of pereopod 3, lateral view; C, pleura of abdominal somites 3-5, lateral view (AS, abdominal somite). P. edwardsii (Brandt, 1851), male, MNRJ 14655 (carapace length 22mm); D, telson and uropods, dorsal view.
FIGURE 5 in Report on some Plesionika Bate, 1888 and first record of Stylopandalus Coutiére, 1905 (Caridea, Pandalidae) from Brazilian waters
FIGURE 5. Plesionika miles (A. Milne Edwards, 1883), male, MNRJ 14661 (carapace length 9mm); A, lateral view; B, right antennule, dorsal view; C, right scaphocerite, dorsal view (as, antennal spine; ps, pterygostomian spine; st, stylocerite); D, right pereopod 2, lateral view; E, left pereopod 2, lateral view.
FIGURE 8 in Report on some Plesionika Bate, 1888 and first record of Stylopandalus Coutiére, 1905 (Caridea, Pandalidae) from Brazilian waters
FIGURE 8.- Stylopandalus richardi (Coutiére, 1905), male, MNRJ 19995 (carapace length 7.2mm); A, left maxilliped 2, dorsal view; B, appendix interna and appendix masculina of right second pleopod, lateral view; C, propod and dactyl of pereopod 3, lateral view; D, pleura of abdominal somites 3–5, lateral view (AS, abdominal somite); E, telson and uropods, dorsal view.
FIGURE 1 in Report on some Plesionika Bate, 1888 and first record of Stylopandalus Coutiére, 1905 (Caridea, Pandalidae) from Brazilian waters
FIGURE 1. Plesionika edwardsii (Brandt, 1851), male, MNRJ 14655 (carapace length 22mm); A, lateral view; B, right antennule, dorsal view; C, right scaphocerite, dorsal view (as, antennal spine; ps, pterygostomian spine); D, right pereopod 2, lateral view; E, left pereopod 2, lateral view.
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