Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
1,694
datasets available to search
ShareScore release 0.9.0
Dataset results
1,694 results for “Weevil”
Fig. 1 in Effect of plant sex (dioecism) on the performance of Apocnemidophorus pipitzi (Coleoptera: Curculionidae), a stem boring weevil of Brazilian peppertree, Schinus terebinthifolia
Fig. 1. Leaf consumption of male and female Brazilian peppertree plants by the weevil Apocnemidophorus pipitzi. Feeding damage was significantly higher on male plants. Asterisk (*) indicates statistical difference (t = 3.05; df = 4; P = 0.027).
Fig. 2 in Effect of plant sex (dioecism) on the performance of Apocnemidophorus pipitzi (Coleoptera: Curculionidae), a stem boring weevil of Brazilian peppertree, Schinus terebinthifolia
Fig. 2. Longevity of the the weevil Apocnemidophorus pipitzi on male and female Brazilian peppertree plants. Survival was significantly higher on male plants. Asterisk (*) indicates statistical difference (t = 2.71; df = 4; P = 0.029).
Fig. 3. A in Differential proteomic analysis of date palm leaves infested with the red palm weevil (Coleoptera: Curculionidae)
Fig. 3. A pie chart presenting the classification of identified proteins according to their biological functions, expressed in percentage.
Fig. 1 in Differential proteomic analysis of date palm leaves infested with the red palm weevil (Coleoptera: Curculionidae)
Fig. 1. Two-dimensional differential gel electrophoresis representative images of date palm proteins. The protein sample of control, wounded, infested, and internal standard (pooled of all the samples) are individually labeled with Cy dyes, mixed together and separated by two-dimensional differential gel electrophoresis followed by image scanning. (A) image of date palm control sample and labeled with cy3 dye; (B) image of date palm artificially wounded sample labeled with cy5 dye; (C) image of date palm sample infested with red palm weevil and labeled with cy3 dye; (D) image of date palm sample pooled from all and labeled with cy2 dye; (E) overlay gel of control, infested, and wounded along with internal standard.
Fig. 2 in Differential proteomic analysis of date palm leaves infested with the red palm weevil (Coleoptera: Curculionidae)
Fig. 2. Venn diagram for the relative distribution of proteins spots in control, mechanically wounded, and red palm weevil infested date palm samples. The non-overlapping segment of diagram represent the number of proteins which were significantly up-regulated (> 1.5-fold) in the corresponding group when compared with the other two groups. The overlapping region between any two groups represents the number of protein spots significantly up-regulated (> 1.5-fold) compared to the third one. The central overlapping region depicts the protein spots where no statistically significant change in up- or down-regulation was observed.
Figs. 7-10 in Development of a training program to identify invasive weevils in the Caribbean basin and the United States
Figs. 7-10. Hands-on student training (7), and weevil identification process (8 and 9), image-based selection of diagnostic characters that leads to species identification in question (10), spreadsheet on a species with embedded brief introduction, distribution, hosts, damage, biological and ecological notes, and bibliography.
Figs. 1-6 in Development of a training program to identify invasive weevils in the Caribbean basin and the United States
Figs. 1-6. Red palm weevil (1), and South American palm weevil (2), South American palm weevil damage (3, 4, 5), and red ring disease symptom (6). Arrows 3 and 4 show early and late infestation of South American palm weevil, arrow 5 shows a full-grown larva and its damage, arrow 6 shows the cross section of coconut palm with red ring disease.
Figs. 1-18 in Emergent and possible invasive pest species of weevils in Mexico
Figs. 1-18. (1) Conotrachelus perseae Barber; (2) Conotrachelus aguacatae Barber; (3) Conotrachelus dimidiatus Champion; (4) Conotrachelus copalensis Salas and Romero; (5) Heilipus lauri (Boheman); (6) Heilipus albopictus (Champion); (7) Copturus aguacatae Kissinger; (8) Sphenophorus incurrens Gyllenhal; (9) Scyphophorus acupunctatus Gyllenhal; (10) Cactophagus spinolae (Gyllenhal); (11) Apinocis subnudus (Buchanan); (12) Rhyssomatus nigerrimus (Fåhraeus); (13) Epicaerus operculatus (Say); (14) Epicaerus cognatus Sharp; (15) Amphidees latifrons (Sharp); (16) Naupactus cervinus (Boheman); (17) Epicaerus aurifer Boheman; (18) Epicaerus mexicanus Boheman.
Fig. 3 in Biology, chemical ecology, and sexual dimorphism of the weevil Myllocerus undecimpustulatus undatus (Coleoptera: Curculionidae)
Fig. 3. Chromatographic detection of volatiles present in headspace of peach flush, mature peach leaves, and Valencia (sweet orange) leaves.
Fig. 4 in Biology, chemical ecology, and sexual dimorphism of the weevil Myllocerus undecimpustulatus undatus (Coleoptera: Curculionidae)
Fig. 4. (A) Antennae of Sri Lankan weevil; (B) scanning electron microscopy of olfactory and mechanoreceptor hairs on the club of Sri Lankan weevil antennae; (C) arrangement of antennal preparation for electroantennogram recordings.
Fig 2 in Biology, chemical ecology, and sexual dimorphism of the weevil Myllocerus undecimpustulatus undatus (Coleoptera: Curculionidae)
Fig 2. Sri Lankan weevil larval distribution in top (black columns) and bottom (gray columns) 5 inches of soil in pots containing peach seedlings. No significant differences were observed in the distribution of larval stages.
Fig. 1 in Biology, chemical ecology, and sexual dimorphism of the weevil Myllocerus undecimpustulatus undatus (Coleoptera: Curculionidae)
Fig. 1. (A) Lateral view showing the difference in size of female and male Sri Lankan weevils. Dimorphism appears as black-gray markings on the ventral mesosternum of female (B) and male weevils (C).
Fig. 3 in Does prior feeding behavior by previous generations of the maize weevil (Coleoptera: Curculionidae) determine future descendants feeding preference and ovipositional suitability?
Fig. 3. Mean (SE) number of S. zeamais (n = 8,000) attracted to corn, barley, brown rice, and white rice, with a 200 µL Eppendorf tube containing the pheromone lure placed in barley. Means with the same letter are not significantly different.
Fig. 1 in The effect of reproductive system on invasiveness: lessons from South American weevils
Fig. 1. Worldwide spatial distribution of mitochondrial and nuclear genetic variation of Naupactus cervinus and Naupactus leucoloma. The lef and right side of the pie chart depicts the mitochondrial and nuclear variants, respectively. Circles are multi-locus genotypes of Naupactus cervinus and squares are multi-locus genotypes of Naupactus leucoloma. Distribution in Argentina of the colonizer genotypes also is indicated in smaller size.
Fig. 6 in Does prior feeding behavior by previous generations of the maize weevil (Coleoptera: Curculionidae) determine future descendants feeding preference and ovipositional suitability?
Fig. 6. Number (SE) of S. zeamais male and female (n = 200) emergence when reared on the individual host grains: corn, barley, brown rice, and white rice. Means with the same letter are not significantly different.
Fig. 5 in Does prior feeding behavior by previous generations of the maize weevil (Coleoptera: Curculionidae) determine future descendants feeding preference and ovipositional suitability?
Fig. 5. Mean (SE) number of S. zeamais (n = 8,000) attracted to corn, barley, brown rice, and white rice, with a 200 µL Eppendorf tube containing the pheromone lure placed in brown rice. Means with the same letter are not significantly different.
Fig. 2 in Does prior feeding behavior by previous generations of the maize weevil (Coleoptera: Curculionidae) determine future descendants feeding preference and ovipositional suitability?
Fig. 2. Mean (SE) number of S. zeamais (n = 8,000) attracted to corn, barley, brown rice, and white rice, with a 200 µL Eppendorf tube containing the pheromone lure placed in corn. Weevils were reared on corn, barley, brown rice, and white rice, then presented with a choice of 4 host grains. Means with the same letter are not significantly different.
Fig. 1 in Does prior feeding behavior by previous generations of the maize weevil (Coleoptera: Curculionidae) determine future descendants feeding preference and ovipositional suitability?
Fig. 1. Mean (SE) number of S. zeamais (n = 8,000) attracted to corn, barley, brown rice, and white rice. Weevils were reared on corn, barley, brown rice, and white rice, then presented with a choice of 4 host grains. Means with the same letter are not significantly different.
Fig. 4 in Does prior feeding behavior by previous generations of the maize weevil (Coleoptera: Curculionidae) determine future descendants feeding preference and ovipositional suitability?
Fig. 4. Mean (SE) number of S. zeamais (n = 8,000) attracted to corn, barley, brown rice, and white rice, with a 200 µL Eppendorf tube containing the pheromone lure placed in white rice. Means with the same letter are not significantly different.
Fig. 2 in The effect of reproductive system on invasiveness: lessons from South American weevils
Fig. 2. Multi-locus genotypes of N. cervinus in locations surrounding the port of Buenos Aires (indicated by ship's wheel (helm) symbol).
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.