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133 results for “functional feed”
FIGURES 53–62 in Immature stages of the Rubiaceae-feeding metalmark butterflies (Lepidoptera: Riodinidae), and a new function for the tentacle nectary organs
FIGURES 53–62. Scanning electron micrographs of the first instar of Mesosemia cippus. 53, lateral view; 54, head in laterodorsal view; 55, prothoracic plate in dorsal view, note that tactile SD1 arises from a pinaculum; 56, setae and perforated cupola organs (PCOs) on segments A1–A4 in lateral view; 57, dorsal setae (D1 and D2) and PCOs (DL1 and DL2) on the metathorax; 58, spiracle on A7 segment; 59, segment A8 in dorsal view, showing the opening (arrow) of tentacle nectary organ (TNO), dorsal setae (D1 and D2), PCOs (DL1 and DL2) and spiracle; 60, TNOs everted; 61, detail of TNO secretion (arrow); 62, proleg in ventral view.
FIGURE 52 in Immature stages of the Rubiaceae-feeding metalmark butterflies (Lepidoptera: Riodinidae), and a new function for the tentacle nectary organs
FIGURE 52. Diagram of the larval body chaetotaxy of the first instar of Mesosemia cippus in lateral view, showing position of setae (black circles) and perforated cupola organs (grey circles).
FIGURES 49–51 in Immature stages of the Rubiaceae-feeding metalmark butterflies (Lepidoptera: Riodinidae), and a new function for the tentacle nectary organs
FIGURES 49–51. Scanning electron micrographs of Mesosemia cippus eggs. 49, lateral view; 50, hexagonal cells of the exochorion; 51, micropylar area (Mp).
FIGURES 41–48. Interactions between Mesosemia cippus immatures and their natural enemies. 41–42 in Immature stages of the Rubiaceae-feeding metalmark butterflies (Lepidoptera: Riodinidae), and a new function for the tentacle nectary organs
FIGURES 41–48. Interactions between Mesosemia cippus immatures and their natural enemies. 41–42, Telenomus sp. (Hymenoptera: Platygastridae) microparasitoid wasps parasitizing (41) and emerging from eggs (42); 43–44, parasitoid cocoon of Hyposoter sp. (Hymenoptera: Ichneumonidae) under fourth instar host remains (43) and adult of Hyposoter sp. (44); 45, adult of Brachymeria sp. (Hymenoptera: Chalcididae); 46, third instar being attacked by a ceratopogonid biting midge (arrow); 47, nymph of a chrysopid (Neuroptera) preying on third instar (arrow); 48, simulated encounter between larva and Camponotus punctulatus ants in the laboratory, note the TNOs everted (arrow).
FIGURES 1–24 in Immature stages of the Rubiaceae-feeding metalmark butterflies (Lepidoptera: Riodinidae), and a new function for the tentacle nectary organs
FIGURES 1–24. Adults of six Mesosemiina species included in this work, in dorsal and ventral views, respectively. 1–4, Mesosemia cippus, male (1–2) and female (3–4) from Villavicencio, Meta, Colombia; 5–8, M. thymetus thymetina, male (5–6) and female (7–8) from Villavicencio; 9–12, M. walteri, male (9–10) and female (11–12) from Villavicencio; 13–16, Leucochimona lagora, male (13–14) and female (15–16) from Villavicencio; 17–20, L. icare matatha, male (17–18) and female (19–20) from Jundiai, São Paulo, Brazil; 21–24, Semomesia croesus lacrimosa, male (21–22) and female (23–24) from Villavicencio.
FIGURES 25–27 in Immature stages of the Rubiaceae-feeding metalmark butterflies (Lepidoptera: Riodinidae), and a new function for the tentacle nectary organs
FIGURES 25–27. Greenhouse built for rearing work (25); detail of host plants set out to attract female Mesosemiina (26); female of Mesosemia cippus ovipositing (arrow) on a cultivated host plant (27).
Raw data_Evaluation of black soldier fly larvae meal as a functional feed ingredient in Atlantic salmon (Salmo salar) under farm-like conditions
Open the record for dataset details and reuse information.
Figure 2 in Functional responses and feeding rates of Mesocyclops pehpeiensis Hu (Copepoda) fed different diets (rotifers, cladocerans, alga and cyanobacteria)
Figure 2. Functional response curves of Mesocyclops pehpeiensis fed Brachionus rubens with (closed circles) and without (open circles) algae at different densities and under different temperature regimes. Replicate data are plotted for each prey concentration. Transformations are based on the Michaelis–Menten equation shown in Material and Methods.
Figure 3 in Functional responses and feeding rates of Mesocyclops pehpeiensis Hu (Copepoda) fed different diets (rotifers, cladocerans, alga and cyanobacteria)
Figure 3. Phytoplankton (Chlorella vulgaris and Anabaena sp.) consumption by adult female Mesocyclops pehpeiensis. Values represent mean ± SE based on four replicates. For each phytoplankton species, data indicated by dissimilar letters are statistically significant (p <0.05, Tukey test).
Figure 1 in Functional responses and feeding rates of Mesocyclops pehpeiensis Hu (Copepoda) fed different diets (rotifers, cladocerans, alga and cyanobacteria)
Figure 1. Prey selectivity index (Manly's α) by the copepod Mesocyclops pehpeiensis offered different prey species at low (0.5 ind. ml−1) and high (2.0 ind. ml−1) densities. Data bars above the horizontal line represent active prey selection.
Figure 10 in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 10. Frame sequences of videos showing feeding behavior. A, Tropisternus latus Brullé, 1837, note that the larvae raise the head out of water while feeding. B, Hydrophilus (Dibolocelus) palpalis Brullé, 1837. C, Hemiosus dejeanii (Solier, 1849). D, Oocyclus magnifica Hebauer & Wang, 1998. See also Supporting Information, Videos S1–S4.
Figure 7 in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 7. Labroclypeal region of Laccobius larvae. A, B, Laccobius kunashiricus Shatrovskiy, 1984, third-instar larva, SEM micrograph, dorsal view: A, labroclypeus; B, left epistomal lobe. C–E, Laccobius (Microlaccobius) sp., third-instar larva, SEM micrograph, dorsal view: C, left epistomal lobe; D; detail of gFR2 setae; E, seta-like cuticular projections of the latero-ventral membranous lobe. Abbreviations: EpLb, epistomal lobe; NS, nasale. Colours: light blue, frontoclypeal region; green, gFR1, group of sensilla of nasale; violet, gFR2, group of sensilla of epistomal lobe.
Figure 4. Piercing-sucking mandibles. A–C in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 4. Piercing-sucking mandibles. A–C, Hybogralius hartmeyeri (Régimbart, 1908), third-instar larva, light microscope photographs, dorsal view: A, left mandible; B, detail of mandibular teeth; C, right mandible. D–F, Epimetopus mendeli Fikáček et al. 2011, first-instar larva, SEM micrograph, dorsal view: D, left mandible; E, detail of mandibular teeth; F, right mandible. Abbreviations: rc1, first retinaculum; rc2, second retinaculum; rc3, third retinaculum; pt, prostheca.
Figure 1 in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 1. Head capsule of larvae with chewing (A–C) and piercing-sucking (D–I) feeding system, SEM micrograph, dorsal view. A, Hydrophilus (Dibolocelus) palpalis Brullé, 1837, second-instar larva. B, Tropisternus setiger Germar, 1824, firstinstar larva. C, Derallus paranensis Oliva, 1981, first instar larva. D, Berosus sp., third-instar larva. E, Hemiosus bruchi Knisch, 1924, third-instar larva. F, Oocyclus iguazu (Oliva 1996), third-instar larva. G, Laccobius kunashiricus Shatrovskiy, 1984, third-instar larva. H, Hybogralius hartmeyeri (Régimbart, 1908), third-instar larva, light microscope photograph. I, Epimetopus mendeli Fikáček et al. 2011, first-instar larva.
Figure 3. Piercing-sucking mandibles. A–C in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 3. Piercing-sucking mandibles. A–C, Berosus patruelis Berg, 1885, first-instar larva, SEM micrograph: A, left mandible, ventral view; B, detail of mandibular teeth, ventral view; C, right mandible, dorsal view. D–F, Laccobius hammondi Gentili, 1984, third-instar larva, SEM micrograph, dorsal view: D, left mandible; E, detail of mandibular teeth; F, right mandible. G–I, Oocyclus iguazu (Oliva, 1996) third-instar larva, SEM micrograph, dorsal view; G, left mandible; H, detail of mandibular teeth; I, right mandible.
Figure 15 in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 15. Phylogeny of the Hydrophiloidea with mapped evolution of tracheal system (A) and mouthparts (B, C). Two alternative ancestral state reconstructions of mouthparts, considering mouthparts of the Pelthydrus-group as: B, piercingsucking; C, chewing (only tribe Laccobiini shown). D, number of species of aquatic genera of Hydrophilidae with known larvae. Colors of branches/bars/pie-charts indicate functional morphology of mouthparts (red = piercing-sucking, blue = chewing, green = filter-feeding) and development of the tracheal system (grey = open; orange = closed).
Figure 6 in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 6. Labroclypeal region of Hemiosus larvae. A, B, Hemiosus bruchi Knisch, 1924, third-instar larva, SEM micrograph, dorsal view: A, labroclypeus; B, left epistomal lobe. C–E, Hemiosus multimaculatus (Jensen-Haarup, 1910), third-instar larva, dorsal view: C, left epistomal lobe, SEM micrograph; D, detail of gFR2 serrated setae, SEM micrograph; E, left epistomal lobe, light microscope photograph. Abbreviations: EpLb, epistomal lobe; NS, nasale. Colours: light blue, frontoclypeal region; green, gFR1, group of sensilla of nasale; violet, gFR2, group of sensilla of epistomal lobe.
Figure 5 in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 5. Labroclypeal region of larvae with chewing feeding system, SEM micrograph, dorsal view. A, Tropisternus acaragua Bachmann, 1969, first-instar larva. B, Hydrochara caraboides (Linnaeus, 1758), first-instar larva. C, Hydrophilus (Dibolocelus) palpalis Brullé, 1837, second-instar larva. D, Derallus paranensis Oliva, 1981, first instar larva. E, Helochares ventricosus Bruch, 1915, first-instar larva. F, Hydroglobus puncticolle Bruch, 1915, third-instar larva. G, Dactylosternum cacti (LeConte, 1855), third-instar larva. H, Cercyon quisquilius (Linnaeus, 1761), third-instar larva, white arrow indicates labroclypeal notch. Colours: light blue, frontoclypeal region; green, gFR1, group of sensilla of nasale; violet, gFR2, group of sensilla of epistomal lobe.
Figure 2 in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 2. Chewing mandibles, SEM micrograph, dorsal view. A, Derallus sp., first-instar larva. B, Enochrus sp., firstinstar larva. C, Tropisternus sp., second-instar larva. D, Hydrophilus (Dibolocelus) palpalis Brullé, 1837, first-instar larva. E, Dactylosternum cacti (LeConte, 1855), third-instar larva. F, Cercyon quisquilius (Linnaeus, 1761), third-instar larva. Abbreviations: rc1, first retinaculum; rc2, second retinaculum; rc3, third retinaculum.
Figure 12 in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 12. Schematic drawing of the piercing-sucking feeding mechanism: 1, sucking channel; 2, epistomal-mandibular coupling system; 3, flexible area.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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