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1,149 results for “plant association”
Figures 63–70 in Revision of the Australian species of Pleistodontes (Hymenoptera: Agaonidae) fig-pollinating wasps and their host-plant associations
Figures 63–70. Antennae (females). (63) P. astrabocheilus sp. nov.; (64) P. proximus; (65) P. imperialis; (66) P. macrocainus sp. nov.; (67) P. greenwoodi; (68) P. cuneatus; (69) P. xanthocephalus sp. nov.; (70) P. athysanus sp. nov.
Figures 71–76 in Revision of the Australian species of Pleistodontes (Hymenoptera: Agaonidae) fig-pollinating wasps and their host-plant associations
Figures 71–76. Head (females). (71) P. proximus gena; (72) P. imperialis clypeus; (73) P. macrocainus sp. nov. clypeus; (74) P. astrabocheilus sp. nov. clypeus; (75) P. athysanus sp. nov. clypeus; (76) P. proximus clypeus. Scale bar = 50 Mm.
Figures 46–52 in Revision of the Australian species of Pleistodontes (Hymenoptera: Agaonidae) fig-pollinating wasps and their host-plant associations
Figures 46–52. (46) P. schizodontus sp. nov. pollen pocket; (47) P. rigisamos pollen pocket; (48) P. schizodontus sp. nov. tergites; (49) P. cuneatus clypeus; (50) P. cuneatus head; (51–52) P. cuneatus mandibles. Scale bar = 100 Mm.
Figures 35–39 in Revision of the Australian species of Pleistodontes (Hymenoptera: Agaonidae) fig-pollinating wasps and their host-plant associations
Figures 35–39. Antenna (females). (35) P. nigriventris; (36) P. addicotti; (37) P. nitens; (38) P. achorus sp. nov.; (39) P. achorus sp. nov. head.
Figures 53–62 in Revision of the Australian species of Pleistodontes (Hymenoptera: Agaonidae) fig-pollinating wasps and their host-plant associations
Figures 53–62. Head (females). (53) P. imperialis mandibles; (54) P. macrocainus sp. nov. mandibles; (55) P. proximus mandibles; (56) P. astrabocheilus sp. nov. mandibles; (57) P. imperialis head; (58) P. macrocainus sp. nov. head; (59) P. astrabocheilus sp. nov. head; (60) P. athysanus sp. nov. head; (61) P. athysanus sp. nov. mandibles and gena; (62) P. proximus head. Scale bar = 100 Mm.
Figures 9–13 in Revision of the Australian species of Pleistodontes (Hymenoptera: Agaonidae) fig-pollinating wasps and their host-plant associations
Figures 9–13. Antennae (females). (9) P. rigisamos; (10) P. schizodontus; (11) P. froggatti; (12) P. deuterus sp. nov.; (13) P. regalis.
Figures 29–34 in Revision of the Australian species of Pleistodontes (Hymenoptera: Agaonidae) fig-pollinating wasps and their host-plant associations
Figures 29–34. Pollen pocket. (29) P. froggatti; (30) P. regalis; (31) P. deuterus sp. nov.; (32) P. nigriventris; (33) P. addicotti; (34) P. nitens. Scale bar = 50 Mm.
Figures 40–45 in Revision of the Australian species of Pleistodontes (Hymenoptera: Agaonidae) fig-pollinating wasps and their host-plant associations
Figures 40–45. Head (females). (40) P. schizodontus; (41) P. rigisamos; (42) P. schizodontus sp. nov. clypeus; (43) P. rigisamos clypeus; (44) P. schizodontus sp. nov. mandibles; (45) P. rigisamos mandibles. Scale bar = 100 Mm.
Figures 14–22 in Revision of the Australian species of Pleistodontes (Hymenoptera: Agaonidae) fig-pollinating wasps and their host-plant associations
Figures 14–22. (14) P. regalis pronotum anterior part; (15) P. nitens metasoma; (16) P. addicotti head; (17) P. nitens head; (18) P. nigriventris head; (19) P. addicotti mandibular appendages; (20) P. nitens mandibular appendages; (21) P. nitens mandibles (22) P. nigriventris mandibular appendages. Scale bar = 200 Mm, except 14 & 22 = 100 Mm.
Figures 77–82 in Revision of the Australian species of Pleistodontes (Hymenoptera: Agaonidae) fig-pollinating wasps and their host-plant associations
Figures 77–82. Head and mesosoma (females). (77) P. macrocainus sp. nov. vertex; (78) P. cuneatus pollen pocket; (79) P. astrabocheilus sp. nov. pollen pocket; (80) P. macrocainus sp. nov. pollen pocket; (81) P. greenwoodi pollen pocket; (82) P. xanthocephalus sp. nov. pollen pocket. Scale bar = 100 Mm.
Figures 88–91 in Revision of the Australian species of Pleistodontes (Hymenoptera: Agaonidae) fig-pollinating wasps and their host-plant associations
Figures 88–91. (88) P. macrocainus sp. nov. (ex F. brachypoda) mandible; (89) P. greenwoodi mandible; (90) P. greenwoodi fore leg; (91) P. xanthocephalus sp. nov. fore leg. Scale bar = 50 Mm.
Figures 1–8 in Revision of the Australian species of Pleistodontes (Hymenoptera: Agaonidae) fig-pollinating wasps and their host-plant associations
Figures 1–8. Head (females). (1) P. froggatti dorsal view; (2) P. froggatti mandibles; (3) P. deuterus sp. nov. dorsal view; (4) P. regalis dorsal view; (5) P. froggatti clypeus; (6) P. deuterus sp. nov. clypeus; (7) P. regalis clypeus; (8) P. regalis mandibles. Scale bar = 200 Mm (head) and 50 Mm (clypeus and mandibles).
[Data from:] Hypersensitive-like response in Brassica plants is specifically induced by molecules from egg-associated secretions of cabbage white butterflies
<p>Characterization at physiological and molecular level of a HR-like cell death induced by <em>Pieris </em>spp. butterfly eggs in <em>Brassica</em> plants.</p>
Mapping of solar panels and Fukushima Daiichi Nuclear Power Plant Accident-associated radioactive waste storage in 2022 and 2023, Fukushima, Japan
<p>The policy of reconstruction after the Fukushima Daiichi Nuclear Plant accident has led to a radical transformation of the landscapes of Fukushima Prefecture especially in two aspects (Asanuma-Brice et al., 2023). The first is related to an extensive decontamination policy which resulted in the removal of more than 13 million m<sup>3</sup> of contaminated soil (MOEJ, 2021). The second is the widespread installation of solar panels, which demonstrate the transition decided by the Prefecture and the inhabitants in terms of energy policy.</p> <p>A systematic mapping of these features was carried out from the satellite imagery of Google Map (2023) within the boundaries of Fukushima Prefecture. The objective was to highlight the evolution of specific land use features that are captured imprecisely by automatic detection mapping. We focused on the main visible change in the landscape in terms of land use since Fukushima Daiichi nuclear accident: contaminated waste disposal areas and solar panel fields. These zones were delineated allowing a calculation of the corresponding surface areas (m<sup>2</sup>).<strong> The dataset is composed of 4 shapefile layers: contaminated waste deposits in 2022 and 2023, solar panels in 2022 and 2023. For the year 2022 the last update was conducted in July 2022 and for the year 2023 the last update took place in March 2023.</strong></p> <p>As the land use is in constant and rapid transition (Asanuma-Brice, 2021), we considered as contaminated waste deposits, the permanent storage centers as well as the sites where there are still bags of contaminated waste in varying numbers, knowing that they will be removed and stored on other dedicated sites (Evrard et al., 2019). This choice was made to potentially identify, when the map was updated, the future uses of the land where this waste was stored temporarily.</p> <p>This dataset is part of a larger project that aims to provide the community with an interactive tool (https://mitatelab.cnrs.fr/mitate-labs-map-of-solar-panel-and-contaminated-wasted-land/) that makes available various types of information essential to the analysis of the reconstruction, such as: the delineation of the evacuated zone (which evolved throughout time), the delineation of the municipality boundaries affected by the reconstruction policy, the main services found in these localities, the location of the memorials of the disaster in the zone, as well as the geo-localization of the soil/sediment samples collected by other Mitate lab researchers in order to investigate the redistribution of radionuclides in the environment (Evrard et al., 2021).</p>
Fig 5 in Description and key to the fifth-instars of some Cicadas (Hemiptera: Cicadidae) associated with coffee plants in Brazil
Fig 5 Spines along the length of mid tibia. a) Dorisiana viridis; b) Fidicina mannifera; c) Fidicinoides pronoe. Scales = 1 mm.
Fig 2 in Description and key to the fifth-instars of some Cicadas (Hemiptera: Cicadidae) associated with coffee plants in Brazil
Fig 2 Left foreleg of fifth-instars. a) Dorisiana drewseni, inner view; b) D. drewseni, outer view; c) Dorisiana viridis, outer view; d) Fidicina mannifera, outer view; e) Fidicinoides pronoe, outer view; f) Carineta fasciculata, outer view; g) Quesada gigas, outer view. acf. Accessory tooth of femur; apt. Apical tooth of tibia; bt. Blade of tibia; f. Femur; fc. Femoral comb; itf. Intermediate tooth of femur; pbt. Point of blade of tibia; ptf. Posterior tooth of femur; t. Trochanter; ti. Tibia. Scale = 1 mm.
Fig 3 in Description and key to the fifth-instars of some Cicadas (Hemiptera: Cicadidae) associated with coffee plants in Brazil
Fig 3 Abdominal apex in ventral view. a) Dorisiana drewseni, female; b) D. drewseni, male; c) Dorisiana viridis, male; d) Fidicina mannifera, male; e) Fidicinoides pronoe, male; f) Carineta fasciculata, male; g) Quesada gigas, male. Scales = 1 mm.
Fig 1 Fifth-instars. a in Description and key to the fifth-instars of some Cicadas (Hemiptera: Cicadidae) associated with coffee plants in Brazil
Fig 1 Fifth-instars. a) Dorisiana drewseni, general lateral view of body; b) D. drewseni, dorsal view of head and thorax; c) Dorisiana viridis, general lateral view of body; d) D. viridis, dorsal view of head and thorax; e) Fidicina mannifera, general lateral view of body; f) F. mannifera, dorsal view of head and thorax; g) Fidicinoides pronoe, general lateral view of body; h) F. pronoe, dorsal view of head and thorax; i) Carineta fasciculata, general lateral view of body; j) C. fasciculata, dorsal view of head and thorax. Scale = 3 mm.
Genome-wide association study of aphid abundance highlights a locus affecting plant growth and flowering in Arabidopsis thaliana
<div> <div>Plant life-history traits, such as size and flowering, contribute to shaping variation in herbivore abundance. Although plant genes involved in physical and chemical traits have been well studied, less is known about the loci linking plant life-history traits and herbivore abundance. Here, we conducted a genome-wide association study (GWAS) of aphid abundance in a field population of <em>Arabidopsis thaliana</em>. This GWAS of aphid abundance detected a relatively rare but significant variant on the third chromosome of <em>A. thaliana</em>, which was also suggestively but non-significantly associated with the presence or absence of inflorescence. Out of candidate genes near this significant variant, a mutant of a ribosomal gene (AT3G13882) exhibited slower growth and later flowering than a wild type under laboratory conditions. A no-choice assay with the turnip aphid, <em>Lipaphis erysimi</em>, found that aphids were unable to successfully establish on the mutant. Our genome-wide association study of aphid abundance unexpectedly found a locus affecting plant growth and flowering.</div> </div>
Jumping to new hosts: the diversification of flea beetles (Coleoptera: Chrysomelidae: Alticini) in the context of their host plant associations
<p><span>Flea beetles (Alticini) represent one of the most diverse groups within the family Chrysomelidae and are associated with more than 100 different plant families. Conspicuously, only 10 genera account for about a quarter of flea beetle diversity, whereas about 380 genera each comprise less than ten species, indicating different rates of diversification within the Alticini. Here, we reconstructed the phylogenetic relationships of 608 species in 101 Alticini genera using mitogenomes and cytochrome oxidase I, and applied several frameworks of clade-specific diversification rate analyses. Increased diversification rates were consistently detected in the cosmopolitan genera <em>Altica</em> and <em>Longitarsus</em>, the Palearctic genus <em>Phyllotreta</em>, and in neotropical taxa of the subtribe Oedionychina. In addition, we tested whether the evolution of specialized interactions with plants of the order Brassicales influenced the diversification of <em>Phyllotreta</em> and <em>Psylliodes</em> flea beetles. Specialization on Brassicales was only associated with increased diversification rates in <em>Phyllotreta</em> but not in <em>Psylliodes</em>. Our results indicate that host associations per se do not explain different diversification rates and lay the groundwork for investigating the evolutionary drivers of rapid radiations in Alticini.</span></p>
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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.