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Figure 3 in Effects of different ant species on the attendance of neighbouring hemipteran colonies and the outcomes for the host plant
Figure 3. Proportion of fruit production with (a) Camponotus crassus and (b) Ectatomma tuberculatum in the group with both mealybugs and ants, group with only ants, group with only mealybugs, and group without ants or mealybugs. Two-way analysis of variance (ANOVA, p <0.05) with the presence/absence of each group (ants and mealybugs) treated as a separate factor. Means + 1 standard error (SE) are presented. The asterisk (*) in (a) indicates a significant negative interactive effect by C. crassus and mealybugs on proportion of fruit production (p <0.05; see Table 1).
Figure 3 in The coconut pathosystem: weed hosts of nymphs of the American palm Cixiid Haplaxius crudus (Hemiptera: Fulgoroidea)
Figure 3. Variation of the number of nymphs associated per weed species in the low zone during May 2015–May 2016 in the coconut pathosystem in south-east Mexico.
Figure 2 in The coconut pathosystem: weed hosts of nymphs of the American palm Cixiid Haplaxius crudus (Hemiptera: Fulgoroidea)
Figure 2. Haplaxius crudus fifth instar nymphs on the roots of Panicum laxum, collected 15 February 2015 in the coconut pathosystem in south-east Mexico.
Figure 1 in The coconut pathosystem: weed hosts of nymphs of the American palm Cixiid Haplaxius crudus (Hemiptera: Fulgoroidea)
Figure 1. Haplaxius crudus nymphs in the root and organic material microhabitat in of Digitaria abyssinica, 22 July 2016, in the coconut pathosystem in south-east Mexico.
Figure 1 in Life cycles and host-parasitoid relationships of five species of Leucospis wasps in Argentina (Hymenoptera: Leucospidae)
Figure 1. Location of the sampling sites (SC: San Claudio, AN: Anquilóo and MG: Martín García reserve) within the grasslands of Río de la Plata (the area surrounded by a thick line), with satellite images (altitude 5km), and representative photographs of the different vegetation structure at each site (Satellite images copyright Google Inc. 2013).
Figure 7 in The life history and host-searching behaviour of the aquatic parasitoid wasp Apsilops japonicus (Hymenoptera: Ichneumonidae), a parasitoid of the aquatic moth Neoshoenobia testacealis (Lepidoptera: Crambidae)
Figure 7. Mean number of ovipositor probes into leaf petioles by Apsilops japonicus females for the three types of leaves. There were no significant differences among the three leaf types (n = 36, F = 0.75, P = 0.48, one-way analysis of variance).
Figure 4 in The life history and host-searching behaviour of the aquatic parasitoid wasp Apsilops japonicus (Hymenoptera: Ichneumonidae), a parasitoid of the aquatic moth Neoshoenobia testacealis (Lepidoptera: Crambidae)
Figure 4. Frequency of Apsilops japonicus females entering the water from the three types of leaves (n = 36).
Figure 5 in The life history and host-searching behaviour of the aquatic parasitoid wasp Apsilops japonicus (Hymenoptera: Ichneumonidae), a parasitoid of the aquatic moth Neoshoenobia testacealis (Lepidoptera: Crambidae)
Figure 5. Mean submergence time for Apsilops japonicus females entering the water from the three types of leaves. There were no significant differences among the three leaf types (n = 36, F = 0.45, P = 0.64, one-way analysis of variance).
Figure 2 in The life history and host-searching behaviour of the aquatic parasitoid wasp Apsilops japonicus (Hymenoptera: Ichneumonidae), a parasitoid of the aquatic moth Neoshoenobia testacealis (Lepidoptera: Crambidae)
Figure 2. An Apsilops japonicus larva beside a mature host larva in the petiole. The white bar indicates a parasitoid larva.
Figure 3 in The life history and host-searching behaviour of the aquatic parasitoid wasp Apsilops japonicus (Hymenoptera: Ichneumonidae), a parasitoid of the aquatic moth Neoshoenobia testacealis (Lepidoptera: Crambidae)
Figure 3. Frequency of host stages at oviposition by Apsilops japonicus females. Unknown (n = 3: parasitoid pupa) indicates that we could not discriminate the host stage because the hosts were dead and probably decomposed in the petioles.
Figure 5. Lepeophtheirus acutus Heegaard, 1943 in Redescription of Lepeophtheirus acutus Heegaard, 1943 (Copepoda: Caligidae) parasitic on two elasmobranch hosts off Okinawa-jima Island, Japan
Figure 5. Lepeophtheirus acutus Heegaard, 1943 infections on the Alfred manta Manta alfredi (Krefft, 1868) held in sea pens off the western coastline of Okinawa-jima Island, Japan. (A) Clusters of L. acutus (indicated by arrowheads) around the left eye of M. alfredi (no. 21) on 5 October 2009; and (B) clusters of L. acutus (indicated by arrowheads) on and around the underside of the pelvic fins of M. alfredi (no. 22) on 29 September 2009.
Figure 3. Lepeophtheirus acutus Heegaard, 1943 in Redescription of Lepeophtheirus acutus Heegaard, 1943 (Copepoda: Caligidae) parasitic on two elasmobranch hosts off Okinawa-jima Island, Japan
Figure 3. Lepeophtheirus acutus Heegaard, 1943, adult female (A–C) and adult male (D–G). (A) Left leg 3, ventral; (B) left leg 4, ventral; (C) left leg 5, ventral; (D) habitus, dorsal; (E) right antenna, ventral; (F) left maxillule (MX1) and postoral process (POP), ventral; (G) left maxilliped (arrowhead indicates ornamentation on myxal area), posterior. Scale bars: A = 200 µm; B = 100 µm; C, E–G = 50 µm; D = 400 µm.
Figure 1. Lepeophtheirus acutus Heegaard, 1943 in Redescription of Lepeophtheirus acutus Heegaard, 1943 (Copepoda: Caligidae) parasitic on two elasmobranch hosts off Okinawa-jima Island, Japan
Figure 1. Lepeophtheirus acutus Heegaard, 1943, adult female. (A) Habitus, dorsal; (B) junction of genital complex and abdomen (gp, gonopore; s, spermatophore; arrowhead, copulatory pore), ventral; (C) left caudal ramus, ventral; (D) right antennule, ventral; (E) right antenna, ventral; (F) right postantennal process, ventral; (G) right mandible, posterior; (H) right maxillule, ventral. Scale bars: A = 1.00 mm; B, D, E, H = 100 µm; C, F, G = 50 µm.
Figure 6. Lepeophtheirus acutus Heegaard, 1943 in Redescription of Lepeophtheirus acutus Heegaard, 1943 (Copepoda: Caligidae) parasitic on two elasmobranch hosts off Okinawa-jima Island, Japan
Figure 6. Lepeophtheirus acutus Heegaard, 1943 infections on an Alfred manta Manta alfredi (Krefft, 1868) held in a sea pen off the western coastline of Okinawa-jima Island, Japan. (A) Clusters of L. acutus (indicated by arrowheads) around the mouth and on the left cephalic fin of M. alfredi (no. 22) on 15 November 2009; and (B) large lesion (indicated by arrowhead) on the dorsal body surface of M. alfredi (no. 22) caused by L. acutus on 15 November 2009.
Figure 4. Lepeophtheirus acutus Heegaard, 1943 in Redescription of Lepeophtheirus acutus Heegaard, 1943 (Copepoda: Caligidae) parasitic on two elasmobranch hosts off Okinawa-jima Island, Japan
Figure 4. Lepeophtheirus acutus Heegaard, 1943, adult male (A, B, E, F) and adult female (C, D). (A) Sternal furca, ventral; (B) right legs 5 and 6 with detail of distolateral corner of genital operculum, ventral; (C) endopod of right leg 1, anterior; (D) sternal furca, dorsal; (E) endopod of left leg 3, ventral; (F) distolateral corner of left genital operculum, ventral. Scale bars: A, B, E = 50 µm; C = 25 µm; D = 100 µm; F = 20 µm.
Figure 7. Lepeophtheirus acutus Heegaard, 1943 in Redescription of Lepeophtheirus acutus Heegaard, 1943 (Copepoda: Caligidae) parasitic on two elasmobranch hosts off Okinawa-jima Island, Japan
Figure 7. Lepeophtheirus acutus Heegaard, 1943 infections on the whale shark Rhincodon typus Smith, 1828 held in sea pens off the western coastline of Okinawa-jima Island, Japan. (A) Two ovigerous females of L. acutus (indicated by arrowheads) on the right eye of R. typus (no. 27) on 28 April 2010; and (B) cluster of L. acutus (two individuals in this cluster indicated by arrowheads) associated with a lesion on the dorsal body surface of R. typus (no. 33) on 5 October 2009.
Figure 2. Lepeophtheirus acutus Heegaard, 1943 in Redescription of Lepeophtheirus acutus Heegaard, 1943 (Copepoda: Caligidae) parasitic on two elasmobranch hosts off Okinawa-jima Island, Japan
Figure 2. Lepeophtheirus acutus Heegaard, 1943, adult female. (A) Left maxilla, anterior; (B) left maxilliped, posterior; (C) sternal furca, ventral; (D) right leg 1 with detail of endopod tip and apical armature elements on second exopodal segment, anterior; (E) right leg 2, anterior. Scale bars: A–D = 100 µm; E = 200 µm.
Figure 1 in Diversity and nectar hosts of flower-settling moths within a Florida sandhill ecosystem
Figure 1. Photographic documentation of settling behaviour: (A) Synchlora frondaria (Geometridae) on Balduina angustifolia (Asteraceae); (B) Idaea ostentaria (Geometridae) on Eriogonum tomentosum (Polygonaceae); (C) Hormoschista latipalpus (Noctuidae) on E. tomentosum; (D) Herpetogramma bipunctalis (Crambidae) on Liatris tenuifolia (Asteracaea); (E) Samea ecclesialis (Crambidae) on Ageratina aromatica (Asteraceae); (F) Schinia sanguinea (Noctuidae) on L. tenuifolia.
Figure 2 in Diversity and nectar hosts of flower-settling moths within a Florida sandhill ecosystem
Figure 2. Species of moths observed taking nectar on Ageratina aromatica, including number of individual moths sampled with and without pollen. Two individuals observed but not sampled and not included in graph were Scopula loutaria (Geometridae) and Leucania scirpicola (Noctuidae).
Figure 1 in Potential host range of myrmecophilous Arhopala butterflies (Lepidoptera: Lycaenidae) feeding on Macaranga myrmecophytes
Figure 1. Mean (± SD) forewing length (mm) of male (left) and female (right) adults of Arhopala amphimuta reared from the second-instar larval stage in the laboratory on apical leaves of four Macaranga species: M. winkleri (win), M. trachyphylla (tra), M. beccariana (bec) and M. rufescens (ruf). The numbers of butterflies per Macaranga species are shown in parentheses below the plant name.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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.