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3,370 results for “jumping”
Figure 4 in Jumping plant-lice of the family Phacopteronidae (Hemiptera: Psylloidea) from Cameroon
Figure 4. Pseudophacopteron spp. (A) P. cuniculus; (B) P. nothospondiadis; (C) P. fuscivenosum; (D) P. electum; (E) P. morion; (F) P. lecaniodisci; (G) P. pusillum; (H) P. eastopi. (A–H) Antenna. Scale bars: a (A–D, F–H); b (E).
Figure 8 in Jumping plant-lice of the family Phacopteronidae (Hemiptera: Psylloidea) from Cameroon
Figure 8. Pseudophacopteron spp. (A) P. cuniculus; (B) P. kala; (C) P. nothospondiadis; (D) P. fuscivenosum; (E) P. electum; (F) P. morion; (G) P. lecaniodisci; (H) P. pusillum; (I) P. eastopi. (A–I) Male terminalia, in profile. Scale bars: a (A); b (B–E, G–I); c (F).
Figure 15 in Jumping plant-lice of the family Phacopteronidae (Hemiptera: Psylloidea) from Cameroon
Figure 15. Pseudophacopteron nothospondiadis, fifth instar larva: left dorsal and right ventral surfaces.
Figure 16 in Jumping plant-lice of the family Phacopteronidae (Hemiptera: Psylloidea) from Cameroon
Figure 16. Pseudophacopteron fuscivenosum, fifth instar larva: left dorsal and right ventral surfaces.
Figure 12 in Jumping plant-lice of the family Phacopteronidae (Hemiptera: Psylloidea) from Cameroon
Figure 12. Pseudophacopteron spp. (A) P. fuscivenosum; (B) P. electum; (C) P. morion; (D) P. lecaniodisci; (E) P. eastopi; (F) P. pusillum. (A–F) Female terminalia, in profile. Scale bars: a (A, B, D–F); b (C).
Figure 11 in Jumping plant-lice of the family Phacopteronidae (Hemiptera: Psylloidea) from Cameroon
Figure 11. Pseudophacopteron spp. (A) P. cuniculus; (B) P. kala; (C) P. nothospondiadis. (A–C) Female terminalia, in profile. Scale bars: a (A); b (B, C).
Figure 19 in Jumping plant-lice of the family Phacopteronidae (Hemiptera: Psylloidea) from Cameroon
Figure 19. Pseudophacopteron lecaniodisci, fifth instar larva: left dorsal and right ventral surfaces.
Figure 10 in Jumping plant-lice of the family Phacopteronidae (Hemiptera: Psylloidea) from Cameroon
Figure 10. Pseudophacopteron spp. (A) P. cuniculus; (B) P. kala; (C) P. nothospondiadis; (D) P. fuscivenosum; (E) P. electum; (F) P. morion; (G) P. lecaniodisci; (H) P. pusillum; (I) P. eastopi. (A–I) Distal segment of aedeagus, in profile. Scale bars: a (A–E, G–I); b (F).
Figure 3 in Jumping plant-lice of the family Phacopteronidae (Hemiptera: Psylloidea) from Cameroon
Figure 3. Pseudophacopteron spp. (A, B) P. cuniculus; (C, D) P. nothospondiadis. (A) Antennal segments 3–4; (B) apex of antennal segment 4 with multiple rhinaria; (C) antennal segments 4–5; (D) apex of antennal segment 5 with single rhinarium. Scale bars: 0.03 mm (A); 0.005 mm (B, D); 0.01 mm (C).
Figure 7 in Jumping plant-lice of the family Phacopteronidae (Hemiptera: Psylloidea) from Cameroon
Figure 7. Pseudophacopteron spp. (A) P. cuniculus; (B) P. kala; (C) P. nothospondiadis; (D) P. fuscivenosum; (E) P. electum; (F) P. morion; (G) P. lecaniodisci; (H) P. pusillum; (I) P. eastopi. (A–I) Fore wings, distribution of surface spinules (delimited by dashed lines).
Jumping the green wall: the use of PNA-DNA clamps to enhance microbiome sampling depth in wildlife microbiome research
As microbiome research moves away from model organisms to wildlife, new challenges for microbiome high throughput sequencing arise caused by the variety of wildlife diets. High levels of contamination are commonly observed emanating from the host (mitochondria) or diet (chloroplast). Such high contamination levels affect the overall sequencing depth of wildlife samples thus decreasing statistical power and leading to poor performance in downstream analysis. We developed an amplification protocol utilizing PNA-DNA clamps to maximize the use of resources and to increase the sampling depth of true microbiome sequences in samples with high levels of plastid contamination. We chose two study organisms, a bat (Leptonyteris yerbabuenae) and a bird (Mimus parvulus), both relying on heavy plant-based diets that sometimes lead to traces of plant-based faecal material producing high contamination signals from chloroplasts and mitochondria. On average, our protocol yielded a 13-fold increase in bacterial sequence amplification compared with the standard protocol (Earth Microbiome Protocol) used in wildlife research. For both focal species, we were able significantly to increase the percentage of sequences available for downstream analyses after the filtering of plastids and mitochondria. Our study presents the first results obtained by using PNA-DNA clamps to block the PCR amplification of chloroplast and mitochondrial DNA from the diet in the gut microbiome of wildlife. The method involves a cost-effective molecular technique instead of the filtering out of unwanted sequencing reads. As 33% and 26% of birds and bats, respectively, have a plant-based diet, the tool that we present here will optimize the sequencing and analysis of wild microbiomes.
Figs 87–90 in Jumping plant-lice of Socotra Island (Hemiptera: Psylloidea)
Figs 87–90. Pauropsylla jarmilarum sp. nov., fifth instar immature. 87 – body, left dorsal view with details of lanceolate setae on cephaloprothorax, forewing pad and abdomen, right ventral view; 88 – antenna; 89 – detail of tibiotarsus apex; 90 – detail of circumanal pore ring (right side only).
Figs 91–95 in Jumping plant-lice of Socotra Island (Hemiptera: Psylloidea)
Figs 91–95. Pauropsylla jarmilarum sp. nov. on its host plant, Ficus vasta. 91 – adult male; 92 – leaf with galls; 93 – detail of upper leaf surface with galls; 94 – detail of lower leaf surface with galls and immatures; 95 – Ficus vasta tree in Kazazhan near Homhil. Photographs by V. Hula and J. Niedobová (91–94) and J. Hájek (95).
Figs 74–77 in Jumping plant-lice of Socotra Island (Hemiptera: Psylloidea)
Figs 74–77. Pauropsylla jarmilarum sp. nov., adult and habitat. 74 – habitus, lateral view; 75 – head, frontal view (slide-mounted); 76 – forewing; 77 – sink holes with limestone rocks on plateau in Kazazhan near Homhil area with Ficus vasta (broad-leaved trees in centre), habitat of P. jarmilarum sp. nov. (photograph by J. Hájek).
Figs 78–86 in Jumping plant-lice of Socotra Island (Hemiptera: Psylloidea)
Figs 78–86. Pauropsylla jarmilarum sp. nov., adult. 78 – male terminalia, outer lateral view; 79 – male proctiger, posterior view; 80 – paramere, lateral view, inner face; 81 – distal segment of aedeagus, lateral view; 82 – antenna; 83 – antennal segments 9 and 10; 84 – female terminalia, lateral view, with detail of circumanal ring structure; 85 – female subgenital plate, ventral view; 86 – detail of dorsal and apex of ventral valvulae, lateral view.
Figs 56–62 in Jumping plant-lice of Socotra Island (Hemiptera: Psylloidea)
Figs 56–62. Diaphorina hagherensis sp. nov., adult. 56 – male terminalia, outer lateral view; 57 – paramere, lateral view, inner face; 58 – distal segment of aedeagus, lateral view; 59 – female terminalia, lateral view, with detail of circumanal ring structure; 60 – detail of dorsal and apex of ventral valvulae, lateral view; 61 – antenna; 62 – antennal segments 9 and 10.
Figs 27–33 in Jumping plant-lice of Socotra Island (Hemiptera: Psylloidea)
Figs 27–33. Diaphorina caliginosa sp. nov., adult. 27 – male terminalia, outer lateral view; 28 – paramere, lateral view, inner face; 29 – distal segment of aedeagus, lateral view; 30 – female terminalia, lateral view, with detail of circumanal ring structure; 31 – detail of dorsal and apex of ventral valvulae, lateral view; 32 – antenna; 33 – antennal segments 9 and 10.
Figs 6–9 in Jumping plant-lice of Socotra Island (Hemiptera: Psylloidea)
Figs 6–9. Colposcenia dioscoridis sp. nov, adult. 6 – male, forewing; 7 – female, forewing; 8 – head, dorsal view; 9 – detail of forewing membrane in cell m1 at M-fork.
Figs 49–55 in Jumping plant-lice of Socotra Island (Hemiptera: Psylloidea)
Figs 49–55. Diaphorina elegans Burckhardt & Mifsud, 1998, adult. 49 – male terminalia, outer lateral view; 50 – paramere, lateral view, inner face; 51 – distal segment of aedeagus, lateral view; 52 – female terminalia, lateral view, with detail of circumanal ring structure; 53 – detail of dorsal and apex of ventral valvulae, lateral view; 54 – antenna; 55 – antennal segments 9 and 10.
Figs 18–22 in Jumping plant-lice of Socotra Island (Hemiptera: Psylloidea)
Figs 18–22. Diaphorina caliginosa sp. nov., adult. 18 – habitus, lateral view; 19 – habitus, dorsal view; 20 – forewing; 21 – detail of forewing membrane in cell m1 at M-fork; 22 – head, dorsal view.
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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.