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124 results for “sea lice”
Fig. 25. Anuretes quadrilaterus Shiino, female. A. leg 2. B. leg 3. C. leg 4 in Sea lice (Copepoda, Siphonostomatoida, Caligidae) new to Korea, including three new species
Fig. 25. Anuretes quadrilaterus Shiino, female. A. leg 2. B. leg 3. C. leg 4. Scales=A. 0.2 mm. B, C. 0.1 mm.
Fig. 23. Lepeophtheirus gusevi n in Sea lice (Copepoda, Siphonostomatoida, Caligidae) new to Korea, including three new species
Fig. 23. Lepeophtheirus gusevi n. sp., female. A. leg 4. B. juction between second and third exopodal segment of leg 4. C. leg 5. Male. D. habitus, dorsal. E. genital somite and abdomen, dorsal. F. antenna. G. maxillule. H. maxilliped. Scales=A, C, E. 0.2 mm. B, F-H. 0.1 mm. D. 0.5 mm.
Fig. 27. Pseudanuretes chaetodontis Yamaguti, female. A. habitus, dorsal. B. cephalic area, ventral. C. caudal ramus, ventral. D. antennule. E. antenna and maxillule. F. postantennal process. G in Sea lice (Copepoda, Siphonostomatoida, Caligidae) new to Korea, including three new species
Fig. 27. Pseudanuretes chaetodontis Yamaguti, female. A. habitus, dorsal. B. cephalic area, ventral. C. caudal ramus, ventral. D. antennule. E. antenna and maxillule. F. postantennal process. G. maxilla and maxillary whip. Scales=A, B. 0.1 mm. C-G. 0.02 mm.
Fig. 18 in Sea lice (Copepoda, Siphonostomatoida, Caligidae) new to Korea, including three new species
Fig. 18. Lepeophtheirus parvulus Shiino, female, A. leg 2. B. leg 3. C. leg 4. Male. D. habitus, dorsal. E. genital somite and abdomen, dorsal. F. antenna. G. maxillule. H. maxilliped. Scales=A-C, E-H. 0.1 mm. D. 0.5 mm.
Fig. 3. Caligus equulae Nordmann, female. A. habitus, dorsal. B. urosome, dorsal. C. antennule. D. antenna. E. postantennal process. F. maxillule. G. maxilla. H. maxilliped. I. sternal furca. J. leg 1 in Sea lice (Copepoda, Siphonostomatoida, Caligidae) new to Korea, including three new species
Fig. 3. Caligus equulae Nordmann, female. A. habitus, dorsal. B. urosome, dorsal. C. antennule. D. antenna. E. postantennal process. F. maxillule. G. maxilla. H. maxilliped. I. sternal furca. J. leg 1. Scales=A. 0.2 mm. B. 0.1 mm. C-J. 0.05 mm.
Fig. 12. Pseudocaligus longipes n in Sea lice (Copepoda, Siphonostomatoida, Caligidae) new to Korea, including three new species
Fig. 12. Pseudocaligus longipes n. sp., female. A. sternal furca. B. leg 3. C. leg 4. Male. D. habitus, dorsal. E. urosome, dorsal. F. antenna. G. maxilliped. H. legs 5 and 6. Scales=A-C, F-H. 0.05 mm. D. 0.5 mm. E. 0.1 mm.
Fig. 1. Caligus elongatus Nordmann, female. A. habitus, dorsal. B. abdomen, ventral. C. antennule. D. antenna. E. postantennary process. F. mandible. G. maxillule. H. maxilla. I. maxilliped. J in Sea lice (Copepoda, Siphonostomatoida, Caligidae) new to Korea, including three new species
Fig. 1. Caligus elongatus Nordmann, female. A. habitus, dorsal. B. abdomen, ventral. C. antennule. D. antenna. E. postantennary process. F. mandible. G. maxillule. H. maxilla. I. maxilliped. J. sternal furca. Scales=A. 1 mm. B. 0.2 mm. C-J. 0.1 mm.
Fig. 28. Pseudanuretes chaetodontis Yamaguti, female. A. maxilliped. B. leg 1. C. leg 2. D. leg 3. E. leg 4. F. legs 5 and 6 in Sea lice (Copepoda, Siphonostomatoida, Caligidae) new to Korea, including three new species
Fig. 28. Pseudanuretes chaetodontis Yamaguti, female. A. maxilliped. B. leg 1. C. leg 2. D. leg 3. E. leg 4. F. legs 5 and 6. Scales=A. 0.05 mm. B-F. 0.02 mm.
Fig. 21. Lepeophtheirus gusevi n in Sea lice (Copepoda, Siphonostomatoida, Caligidae) new to Korea, including three new species
Fig. 21. Lepeophtheirus gusevi n. sp., female. A. habitus, dorsal. B. abdomen, dorsal. C. antennule. D. antenna. E. postantennal process. F. mandible. G. maxillule. H, I. maxilla. Scales=A. 1 mm. B, D, E, G, H. 0.2 mm. C, F, I. 0.1 mm.
Fig. 17. Lepeophtheirus parvulus Shiino, female. A. habitus, dorsal. B. abdomen, ventral. C. antennule. D in Sea lice (Copepoda, Siphonostomatoida, Caligidae) new to Korea, including three new species
Fig. 17. Lepeophtheirus parvulus Shiino, female. A. habitus, dorsal. B. abdomen, ventral. C. antennule. D. antenna, postantennal process, and maxillule. E. maxilla. F. maxilliped. G. sternal furca. H. leg 1. Scales=A. 0.5 mm. B-H. 0.1 mm.
Fig. 13 in Sea lice (Copepoda, Siphonostomatoida, Caligidae) new to Korea, including three new species
Fig. 13. Metacaligus uruguyensis (Thomsen), fmale. A. habitus, dorsal. B. abdomen, ventral. C. caudal rami. D. antennule. E. antenna, postantennal process, and maxillule. F. maxilla. G. maxilliped. H. leg 1. Scales=A. 1 mm. B. 0.5 mm. C-F, H. 0.1 mm. G. 0.2 mm.
Fig. 20. Lepeophtheirus tamladus n in Sea lice (Copepoda, Siphonostomatoida, Caligidae) new to Korea, including three new species
Fig. 20. Lepeophtheirus tamladus n. sp., female. A. leg 2. B. leg 3. C. leg 4. Male: D. urosome, dorsal. E. antenna. F. postantennal process. G. maxillule. H. maxilliped. I. legs 5 and 6. Scales=A, C, D, H. 0.1 mm. B, E-G, I. 0.05 mm.
Fig. 8. Caligus laticaudus Shiino, female. A. maxilla. B. leg 3. C. leg 4. D. leg 5. Male. E. habitus, dorsal. F. urosome, ventral. G in Sea lice (Copepoda, Siphonostomatoida, Caligidae) new to Korea, including three new species
Fig. 8. Caligus laticaudus Shiino, female. A. maxilla. B. leg 3. C. leg 4. D. leg 5. Male. E. habitus, dorsal. F. urosome, ventral. G. second and third segments of antenna. Scales=A-C, G. 0.1 mm. D. 0.05 mm. E. 0.5 mm. F. 0.2 mm.
Fig. 16 in Sea lice (Copepoda, Siphonostomatoida, Caligidae) new to Korea, including three new species
Fig. 16. Lepeophtheirus atypicus Lin, Ho and Chen, female. A. leg 2. B. leg 3. C. leg 4. Scales=0.05 mm for all.
Fig. 5. Caligus fistulariae Yamaguti, female. A. habitus, dorsal. B. caudal rami, dorsal. C. antennule. D in Sea lice (Copepoda, Siphonostomatoida, Caligidae) new to Korea, including three new species
Fig. 5. Caligus fistulariae Yamaguti, female. A. habitus, dorsal. B. caudal rami, dorsal. C. antennule. D. antenna, postantennal process, and maxillule. E. maxilla. F. maxilliped. G. sternal furca. H. leg 1. I. distal part of leg 1. Scales=A. 1 mm. B-H. 0.1 mm. I. 0.05 mm.
Fig. 9 in Sea lice (Copepoda, Siphonostomatoida, Caligidae) new to Korea, including three new species
Fig. 9. Caligus rotundigenitalis Yü, female. A. habitus, dorsal. B. caudal rami, dorsal. C. antennule. D. antenna, postantennal process, and maxillule. E. maxilla. F. maxilliped. G. sternal furca. H. leg 1. Scales=A. 0.5 mm. B, D, F. 0.1 mm. C, E, G, H. 0.05 mm.
Fig. 3 in Occurrence of sea lice, Caligus undulatus Shen and Li, 1959 (Copepoda: Siphonostomatoida: Caligidae) in plankton samples collected from Korea
Fig. 3. Caligus undulatus, adult female from Gangjin Bay, Korea. A. genital complex and abodomen, ventral. B. leg 1. C. tip of second exopodal segment of leg 1. D. leg 2. E. leg 3. F. first exopodal segment of leg 3. G, H. leg 4. I. leg 5. Scale bars: A = 200 μm; B-E, G = 100 μm; F, H, I = 50 μm.
Fig. 4 in Occurrence of sea lice, Caligus undulatus Shen and Li, 1959 (Copepoda: Siphonostomatoida: Caligidae) in plankton samples collected from Korea
Fig. 4. Caligus undulatus, adult male from Mokpo Harbour, Korea. A. habitus, dorsal. B. urosome, dorsal. C. antenna. D. postantennal process. E. maxillule. F. post oral pad. G. maxilliped. H. sternal furca. I. genital segment and legs 5 and 6, ventral. Scale bars: A = 400 μm; B, I = 200 μm; C-H = 100 μm.
Fig. 1 in Topical ivermectin is a highly effective seal 'spot-on': A randomised trial of hookworm and lice treatment in the endangered Australian sea lion (Neophoca cinerea)
Fig. 1. Flow diagram of the trial course showing pup recruitment and recapture count for the three experimental groups for each of the three colony visits. P1 = time between recruitment and first recapture; P2 = time between first recapture and second recapture. Observation of deceased pups is shown relative to (i.e., before or after) the pup's sampling at that visit.
Data from: Timing and probability of arrival for sea lice dispersing between salmon farms
<p>Sea lice are a threat to the health of both wild and farmed salmon and an economic burden for salmon farms. With a free-living larval stage, sea lice can disperse tens of kilometers in the ocean between salmon farms, leading to connected sea lice populations that are difficult to control in isolation. In this paper, we develop a simple analytical model for the dispersal of sea lice between two salmon farms. From the model we calculate the arrival time distribution of sea lice dispersing between farms, as well as the level of cross-infection of sea lice. We also use numerical flows from a hydrodynamic model, coupled with a particle tracking model, to directly calculate the arrival time of sea lice dispersing between two farms in the Broughton Archipelago, BC, in order to fit our analytical model and find realistic parameter estimates. Using the parametrized analytical model we show that there is often an intermediate inter-farm spacing that maximizes the level of cross-infection between farms, and that increased temperatures will lead to increased levels of cross-infection.</p>
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