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841 results for “fruit flies”
Transcriptome landscape in fruit flies with mitochondrial methylation deficiency
GEO Series GSE151656. Drosophila melanogaster. 20 samples. Type: Expression profiling by high throughput sequencing.
Pol III transcribed genes, RNA-Seq, female fruit fly, midgut
GEO Series GSE232719. Drosophila melanogaster. 6 samples. Type: Non-coding RNA profiling by high throughput sequencing.
The transcriptional response to the olive fruit fly (Bactrocera oleae) reveals extended differences between tolerant and susceptible olive (Olea europaea L.) varieties
GEO Series GSE81296. Olea europaea. 12 samples. Type: Expression profiling by array.
Figure 4 from: Cruz-Bustos J, Montoya P, Pérez-Lachaud G, Valle-Mora J, Liedo P (2020) Biological attributes of diapausing and non-diapausing Doryctobracon areolatus (Hymenoptera, Braconidae), a parasitoid of Anastrepha spp. (Diptera, Tephritidae) fruit flies. Journal of Hymenoptera Research 78: 41-56. https://doi.org/10.3897/jhr.78.52269
Figure 4 Female survival of Doryctobracon areolatus parasitoids in the fecundity bioassays.
Fig. 8 in The Fruit Flies Of Morocco: New Records Of The Tephritinae (Diptera, Tephritidae)
Fig. 8. Chaetorellia succinea: a — female habitus, dorsal view; b — aculeus.
Enemies make you stronger: Coevolution between fruit fly host and bacterial pathogen increases post-infection survivorship in the host
<p>Multiple laboratory studies have evolved hosts against a non-evolving pathogen to address questions about evolution of immune responses. However, an ecologically more relevant scenario is one where hosts and pathogens can coevolve. Such coevolution between the antagonists, depending on the mutual selection pressure and additive variance in the respective populations, can potentially lead to a different pattern of evolution in the hosts compared to a situation where the host evolves against a non-evolving pathogen. In the present study, we used <em>Drosophila melanogaster</em> as the host and <em>Pseudomonas entomophila</em> as the pathogen. We let the host populations to either evolve against a non-evolving pathogen, or coevolve with the same pathogen. We found that the coevolving hosts on average evolved higher survivorship against the coevolving pathogen and ancestral (non-evolving) pathogen relative to the hosts evolving against a non-evolving pathogen. The coevolving pathogens evolved greater ability to induce host mortality even in non-local (novel hosts) hosts compared to infection by an ancestral (non-evolving) pathogen. Thus, our results clearly show that the evolved traits in the host and the pathogen under coevolution can be different from one-sided adaptation. In addition, our results also show that the coevolving host-pathogen interactions can involve certain general mechanisms in the pathogen, leading to increased mortality induction in non-local or novel hosts. </p>
Map 1 from: El Harym Y, Belqat B (2017) First checklist of the fruit flies of Morocco, including new records (Diptera, Tephritidae). ZooKeys 702: 137-171. https://doi.org/10.3897/zookeys.702.13368
Map 1 - Map showing all collecting sites in Morocco.
Figure 2 from: El Harym Y, Belqat B (2017) First checklist of the fruit flies of Morocco, including new records (Diptera, Tephritidae). ZooKeys 702: 137-171. https://doi.org/10.3897/zookeys.702.13368
Figure 2 - Calotropis procera L., host plant of Dacus longistylus.
Figure 6 from: El Harym Y, Belqat B (2017) First checklist of the fruit flies of Morocco, including new records (Diptera, Tephritidae). ZooKeys 702: 137-171. https://doi.org/10.3897/zookeys.702.13368
Figure 6 - Cynara cardunculus L. host plant of Terellia sp. near longicauda.
Figure 1 from: El Harym Y, Belqat B (2017) First checklist of the fruit flies of Morocco, including new records (Diptera, Tephritidae). ZooKeys 702: 137-171. https://doi.org/10.3897/zookeys.702.13368
Figure 1 - Argania spinosa L. host plant of Ceratitis capitata.
Figure 5 from: El Harym Y, Belqat B (2017) First checklist of the fruit flies of Morocco, including new records (Diptera, Tephritidae). ZooKeys 702: 137-171. https://doi.org/10.3897/zookeys.702.13368
Figure 5 - Onopordum acanthium L. host plant of Tephritis postica.
Figure 4 from: El Harym Y, Belqat B (2017) First checklist of the fruit flies of Morocco, including new records (Diptera, Tephritidae). ZooKeys 702: 137-171. https://doi.org/10.3897/zookeys.702.13368
Figure 4 - Hypochaeris sp., host plant of Ensina sonchi.
Figure 2 in Host effect on morphology of the fruit fly Anastrepha zenildae (Diptera: Tephritidae) from the Semi-Arid region of Rio Grande do Norte
Figure 2. Female of Anastrepha zenildae showing body measurements used to compare flies between hosts and sexes. HW = Head width; FW = Face width; TH = Thorax length; WL = Wing length; WW = Wing width; OVP = Ovipositor length.
Figure 2 from: Leblanc L, Hossain MA, Doorenweerd C, Khan SA, Momen M, San Jose M, Rubinoff D (2019) Six years of fruit fly surveys in Bangladesh: a new species, 33 new country records and discovery of the highly invasive Bactrocera carambolae (Diptera, Tephritidae). ZooKeys 876: 87-109. https://doi.org/10.3897/zookeys.876.38096
Figure 2 Trapping locations in the various Bangladesh surveys (2013–2018).
Figure 6 from: Leblanc L, Hossain MA, Doorenweerd C, Khan SA, Momen M, San Jose M, Rubinoff D (2019) Six years of fruit fly surveys in Bangladesh: a new species, 33 new country records and discovery of the highly invasive Bactrocera carambolae (Diptera, Tephritidae). ZooKeys 876: 87-109. https://doi.org/10.3897/zookeys.876.38096
Figure 6 Zeugodacus madhupurisp. nov.A head B head and scutum C–D abdomen.
Figure 7 from: Leblanc L, Hossain MA, Doorenweerd C, Khan SA, Momen M, San Jose M, Rubinoff D (2019) Six years of fruit fly surveys in Bangladesh: a new species, 33 new country records and discovery of the highly invasive Bactrocera carambolae (Diptera, Tephritidae). ZooKeys 876: 87-109. https://doi.org/10.3897/zookeys.876.38096
Figure 7 Zeugodacus madhupuri sp. nov. A wing B lateral view C terminal abdominal segment.
Figure 7 from: Leblanc L, Doorenweerd C, Jose MS, Pham HT, Rubinoff D (2018) Descriptions of four new species of Bactrocera and new country records highlight the high biodiversity of fruit flies in Vietnam (Diptera, Tephritidae, Dacinae). ZooKeys 797: 87-115. https://doi.org/10.3897/zookeys.797.29138
Figure 7 - Bactrocera (Asiadacus) connecta : lateral view.
Figure 1 in A Survey of Fruit Flies (Diptera: Tephritidae: Dacinae) and their Opiine Parasitoids (Hymenoptera: Braconidae) in Palau
Figure 1. Male lure trap crafted from urine sample cup used in the 2014 survey.
Figure 1 in Additions to the Fruit Fly Fauna (Diptera: Tephritidae: Dacinae) of Bangladesh, with a Key to the Species
Figure 1. Location of collection sites in Bangladesh.
Figure 1 in Trapping Records of Fruit Fly Pest Species (Diptera: Tephritidae) on Oahu (Hawaiian Islands): Analysis of Spatial Population Trends
Figure 1. Map of trapping sites on Oahu (2006–2008), with habitat at each site.
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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.