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Figure 17 in A morphological phylogeny for four families of amblyceran lice (Phthiraptera: Amblycera: Menoponidae, Boopiidae, Laemobothriidae, Ricinidae)
Figure 17. Male genitalia with parameres (shaded), in (A) Chapinia, with basal apodome (b) indicated, (B) Plegadiphilus, (C) Colpocephalum, (D) Menopon, (E) Latumcephalum, showing mesosomal arch (m) (shaded), and (F) Ricinus.
Figure 7 in A morphological phylogeny for four families of amblyceran lice (Phthiraptera: Amblycera: Menoponidae, Boopiidae, Laemobothriidae, Ricinidae)
Figure 7. Forms of the tentorial bridge in (A) Actornithophilus, (B) Ricinus, (C) Odoriphila, and (D) Dennyus.
Figure 16 in A morphological phylogeny for four families of amblyceran lice (Phthiraptera: Amblycera: Menoponidae, Boopiidae, Laemobothriidae, Ricinidae)
Figure 16. Female terminalia of (A) Boopia, with gonapophyses (g), (B) Osborniella, (C) Ancistrona, and (D) Numidicola.
Figure 5 in A morphological phylogeny for four families of amblyceran lice (Phthiraptera: Amblycera: Menoponidae, Boopiidae, Laemobothriidae, Ricinidae)
Figure 5. Character state evolution with the Menoponidae (clades 'C' and 'D'). Characters which change unambiguously are shown mapped onto the strict consensus tree. Unique changes = Z. For character state descriptions, see Appendix 2.
Figure 6 in A morphological phylogeny for four families of amblyceran lice (Phthiraptera: Amblycera: Menoponidae, Boopiidae, Laemobothriidae, Ricinidae)
Figure 6. Characters of the dorsal head, the dorsal head setae (DHS 8–31) and sensilla (a–e) sensu Clay (1969) from (A) a typical menoponid head, (B) Paraboopia, (C) Colpocephalum, (D) Colimenopon, (E) Austromenopon, and (F) Trochiloecetes.
Figure 3 in A morphological phylogeny for four families of amblyceran lice (Phthiraptera: Amblycera: Menoponidae, Boopiidae, Laemobothriidae, Ricinidae)
Figure 3. Character state evolution within the Ricinidae, Laemobothriidae and Boopiidae. Characters which change unambiguously are shown mapped onto the strict consensus tree. Unique changes = Z. For character state descriptions, see Appendix 2.
Figure 4 in A morphological phylogeny for four families of amblyceran lice (Phthiraptera: Amblycera: Menoponidae, Boopiidae, Laemobothriidae, Ricinidae)
Figure 4. Character state evolution within the Menoponidae (clades 'A' and 'B'). Characters which change unambiguously are shown mapped onto the strict consensus tree. Unique changes = Z. For character state descriptions, see Appendix 2.
Figure 2 in A morphological phylogeny for four families of amblyceran lice (Phthiraptera: Amblycera: Menoponidae, Boopiidae, Laemobothriidae, Ricinidae)
Figure 2. Strict consensus of six equally parsimonious trees recovered from a cladistic analysis using 10 000 random addition replicates. (Length = 650 steps, CI = 0.326, RI = 0.585, HI = 0.683.) Jackknife (33% deletion, bold type) and bootstrap values (> 50%, regular type), each based on 1000 replicates, are shown above the nodes, with Bremer support values (decay indices) shown below. Louse families and major clades within the Menoponidae are indicated.
Figure 1 in A morphological phylogeny for four families of amblyceran lice (Phthiraptera: Amblycera: Menoponidae, Boopiidae, Laemobothriidae, Ricinidae)
Figure 1. Strict consensus of the 24 most-parsimonious trees recovered from a cladistic analysis (1000 random addition replicates) of a morphological data matrix by Clay (1970). (Length = 24 steps, CI = 0.833, RI = 0.833, HI = 0.167.) Data for an outgroup taxon Liposcelis bostrychophilus were added to the original matrix. Bootstrap support (> 50%, 100 replicates) for two main clades of lice ('A' and 'B') is shown. A representative host for each louse family is also indicated.
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>
Fig. 3 in Chewing lice (Phthiraptera) infesting breeding Suliformes (Aves: Aequornithes) of the Arabian Peninsula
Fig. 3. (a) Female Pectinopygus socotranus Timmermann; (b) male Pectinopygus socotranus Timmermann; (c) female Pectinopygus sulae (Rudow); (d) male Pectinopygus sulae (Rudow).
Fig. 1 in Chewing lice (Phthiraptera) infesting breeding Suliformes (Aves: Aequornithes) of the Arabian Peninsula
Fig. 1. Map of the Arabian Peninsula indicating bird collection sites: (1) Socotra cormorant; (2) Brown booby; (3) Masked booby.
Fig. 2 in Chewing lice (Phthiraptera) infesting breeding Suliformes (Aves: Aequornithes) of the Arabian Peninsula
Fig. 2. (a) Female Eidmanniella albescens (Piaget); (b) female Eidmanniella nancyae Ryan & Price.
Figs 8–12 in A review of Afrotropical plant-lice of the genus Moraniella, with description of a new species (Hemiptera: Psylloidea: Psyllidae: Rhinocolinae)
Figs 8–12. Moraniella bella sp. n., adult: (8) ơ terminalia, in profile; (9) distal segment of aedeagus, in profile; (10) ^terminalia, in profile, with detail of circumanal ring; (11) ^valvulae; (12) antennal segment 10. Scale bars = 0.1 mm.
Figs 13–16 in A review of Afrotropical plant-lice of the genus Moraniella, with description of a new species (Hemiptera: Psylloidea: Psyllidae: Rhinocolinae)
Figs 13–16. Moraniella bella sp. n., parasitised fifth instar larva: (13) habitus, ventral surface above, dorsal surface below; (14) caudal plate, dorsal view; arrows indicate the mandibles of chalcidoid parasitoids; (15) detail of caudal plate showing wax pores; (16) lanceolate setae on margin of caudal plate. Scale bar = 0.5 mm in Fig. 13, 0.1 mm in Fig. 14, 0.02 mm in Figs 15, 16.
Figs 1–7 in A review of Afrotropical plant-lice of the genus Moraniella, with description of a new species (Hemiptera: Psylloidea: Psyllidae: Rhinocolinae)
Figs 1–7. Moraniella bella sp. n., adult: (1) habitus ơ, (2) habitus ^(in ethanol), (3) forewing (light field), (4) forewing (dark field) showing extension of surface spinules, (5) head ơ, (6) head ^, (7) antenna. Scale bar = 1.0 mm in Figs 1–4, 0.1 mm in Figs 5–7.
Рис. 1. Основная точка сбора материаΛа, окрестности Ростова-на-Αону. Fig. 1. Location of study area in Rostov-on-Don vicinity. in To the fauna of chewing lice (Insecta: Phthiraptera) of birds (Aves: Falconiformes, Strigiformes) in the Lower Don region, Russia
Рис. 1. Основная точка сбора материаΛа, окрестности Ростова-на-Αону. Fig. 1. Location of study area in Rostov-on-Don vicinity.
Data from: Timing and probability of arrival for sea lice dispersing between salmon farms
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Data from: Next-generation matrices for marine metapopulations: the case of sea lice and salmon farms
Open the record for dataset details and reuse information.
Parasites under pressure: salmon lice may adapt to depth-based preventions in aquaculture
<p>Experiment 1. Vertical distribution of copepodids (mixed family groups) in 80 cm columns over time (min) at two pressures.</p> <p>Experiment 2. Vertical distribution of copepodids (individual families) in 80 cm columns at three pressures.</p> <p>Experiment 2 (traits). For each family: body size, egg string length, estimated fecundity and estimated egg size of mother; development times and column distributions (i.e. proportion of copepodids at top of columns) of offspring.</p>
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.