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.
323
datasets available to search
ShareScore release 0.9.0
Dataset results
323 results for “berries”
FIGURE 4–7. 4 in Recent occurrence of Aphanogmus dictynna (Waterston) (Hymenoptera: Ceraphronidae) in Kenya — an important hyperparasitoid of the coffee berry borer Hypothenemus hampei (Ferrari) (Coleoptera: Curculionidae)
FIGURE 4–7. 4. Female, dorsal mesosoma; 5. Female, lateral mesosoma; 6. Male, genitalia; 7. Female, dorsal metasoma.
FIGURES 8–10. 8 & 9 in Recent occurrence of Aphanogmus dictynna (Waterston) (Hymenoptera: Ceraphronidae) in Kenya — an important hyperparasitoid of the coffee berry borer Hypothenemus hampei (Ferrari) (Coleoptera: Curculionidae)
FIGURES 8–10. 8 & 9. Males, heads in frontal view; 10. Male, fore wing venation. (at same scale of magnification).
FIGURE 1–3 in Recent occurrence of Aphanogmus dictynna (Waterston) (Hymenoptera: Ceraphronidae) in Kenya — an important hyperparasitoid of the coffee berry borer Hypothenemus hampei (Ferrari) (Coleoptera: Curculionidae)
FIGURE 1–3. Female, lateral habitus; 2. Female, head in frontal view; 3. Antennae: A. Female; B. Male.
Fig. 2 in Stephanopachys conicolaFisher (Coleoptera: Bostrichidae) Feeding on Decaying Western Juniper (Juniperus occidentalisHooker) Berries: A Novel Association for Bostrichidae
Fig. 2. Juniperus occidentalis berries damaged (left) by Stephanopachys conicola and undamaged (right).
Data for Green's function eigenvalues and Berry curvature
<p>Data files for Figs. 1B, 1C, 2A and 2B.</p>
Coffee Berry Borer (Hypothenemus hampei Ferrari) trap catch and associated weather variables on Hawaii Island
<p>We sampled flying female CBB adults bi-weekly over a three-year period using red funnel traps baited with an alcohol lure at 14 commercial coffee farms on Hawaii Island to characterize seasonal phenology and the relationship between flight activity and five weather variables. We captured almost 5 million scolytid beetles during the sampling period, with 81-93% of the trap catch comprised of CBB. Of the captured non-target beetles, the majority were tropical nut borer, black twig borer and a species of <i>Cryphalus</i>. Two major flight events were consistent across all three years: an initial emergence from January-April that coincided with early fruit development and a second flight during the harvest season from September-December. A generalized additive mixed model (GAMM) revealed that mean daily air temperature had a highly significant positive correlation with CBB flight; most flight events occurred between 20-26 °C. Mean daily solar radiation also had a significant positive relationship with flight. Flight was positively correlated with maximum daily relative humidity at values below ~94%, and cumulative rainfall up to 100 mm; flight was also positively correlated with maximum daily wind speeds up to ~2.5 m/s, after which activity declined.</p>
FIGURE. Floral habit and structure of C. spongifolia. A. Type specimen in situ with open, spathe limb (apex is reflexed out of view), and green spathe tube (ca. 6 cm long). B. Adjacent plant with inflorescences and prophylls. C. Spadix showing from top: sterile appendix, staminate (male) zone, sterile interstice, and green pistillate (female) zone with tapered, conical form. D. Detail of female zone showing a few basal staminodes. E–G. Berries of the preserved type specimen. G. Dissected berry with orthotropous ovules (some outlined) attached by funicles to parietal placentae (arrows). H. Surface of male zone showing closely-packed synandria. I. Synandria separated to show fused anther sacs beneath apical pores (example in center has 8 pores, 8 anthers) J. Mature fruiting head, with single berry removed to show seed packing and 67 seeds extracted (scale bar units: 1 mm) (Bach Ma NP; type 2020; fruit and seeds 2018). Photos: NVD and PJM. in Colocasia spongifolia sp. nov. (Araceae) in southern China and central Vietnam
FIGURE. Floral habit and structure of C. spongifolia. A. Type specimen in situ with open, spathe limb (apex is reflexed out of view), and green spathe tube (ca. 6 cm long). B. Adjacent plant with inflorescences and prophylls. C. Spadix showing from top: sterile appendix, staminate (male) zone, sterile interstice, and green pistillate (female) zone with tapered, conical form. D. Detail of female zone showing a few basal staminodes. E–G. Berries of the preserved type specimen. G. Dissected berry with orthotropous ovules (some outlined) attached by funicles to parietal placentae (arrows). H. Surface of male zone showing closely-packed synandria. I. Synandria separated to show fused anther sacs beneath apical pores (example in center has 8 pores, 8 anthers) J. Mature fruiting head, with single berry removed to show seed packing and 67 seeds extracted (scale bar units: 1 mm) (Bach Ma NP; type 2020; fruit and seeds 2018). Photos: NVD and PJM.
Draft Genome Manuscript for Curtobacterium sp. Isolated from Berries Surfaced in Commercial Cranberry Bogs in Massachusetts, USA
<p>Annotated genome of Curtobacterium sp. MWU13.2055</p>
Draft Genome Manuscript for Pseudomonas sp. Strain MWU13.3659 Isolated from Berries Surfaced in Commercial Cranberry Bogs in Massachusetts, USA
<p>Annotated genome of Pseudomonas sp. MWU13.3659</p>
FIGURE. Seedlings, seeds, embryos, anthers, and pollen in Dicorynia. A–D. Different stages of development in seedlings of D. paraensis, First eophiles unifoliolate and opposite; E–G. Seed of D. guianensis: E. External surface; F. Endosperm of the longitudinally sectioned seed, note the slightly gelatinous upper region; G. Cotyledon and embryo of longitudinally sectioned seed; H. SEM of seed's testa in D. paraensis; I. SEM of endosperm's surface in D. guianensis (notice the presence of circular perforations); J–K. SEM of the hypocotyl-radicular axis of the seed in D. guianensis and D. paraensis; L. SEM of seed's testa in D. guianensis; M–N. SEM of plumule region in embryo of D. guianensis and D. paraensis (note the developed leaf primordia); O. Apex of anther in longer stamen of D. paraensis, showing 4 sporangia and two pores covered by an apicle; P. Apex of anther in shorter stamen of D. guianensis, at least 9 sporangia; Q. Apex of anther in longer stamen of D. guianensis, 8 sporangia; R. Pollen grains in D. paraensis. A–D: Falcão, M.J. 91; E–G, I–J, L–M: Gentry 63030; H, K, N: Berry, P.E. 7460; O: Amaral, E. 618; P, Q: Unknown collector MO1576407; Scale bar. A–D: 2cm; E–G: 3mm; H–L: 1mm; M–N: 100 μm; O-Q: 200μm; R: 5 μm. in A Taxonomic Revision of the Amazonian Genus Dicorynia (Fabaceae: Dialioideae)
FIGURE. Seedlings, seeds, embryos, anthers, and pollen in Dicorynia. A–D. Different stages of development in seedlings of D. paraensis, First eophiles unifoliolate and opposite; E–G. Seed of D. guianensis: E. External surface; F. Endosperm of the longitudinally sectioned seed, note the slightly gelatinous upper region; G. Cotyledon and embryo of longitudinally sectioned seed; H. SEM of seed's testa in D. paraensis; I. SEM of endosperm's surface in D. guianensis (notice the presence of circular perforations); J–K. SEM of the hypocotyl-radicular axis of the seed in D. guianensis and D. paraensis; L. SEM of seed's testa in D. guianensis; M–N. SEM of plumule region in embryo of D. guianensis and D. paraensis (note the developed leaf primordia); O. Apex of anther in longer stamen of D. paraensis, showing 4 sporangia and two pores covered by an apicle; P. Apex of anther in shorter stamen of D. guianensis, at least 9 sporangia; Q. Apex of anther in longer stamen of D. guianensis, 8 sporangia; R. Pollen grains in D. paraensis. A–D: Falcão, M.J. 91; E–G, I–J, L–M: Gentry 63030; H, K, N: Berry, P.E. 7460; O: Amaral, E. 618; P, Q: Unknown collector MO1576407; Scale bar. A–D: 2cm; E–G: 3mm; H–L: 1mm; M–N: 100 μm; O-Q: 200μm; R: 5 μm.
Experimental Gxx, Gxy raw data and a Mathematica script for calculation of Berry's phase
<p>These raw data files supplement our study of Berry's phase in ABA-trilayer graphene.</p>
Raw data of the manuscript: Heterogeneous Freezing of Liquid Suspensions Including Juices and Extracts from Berries and Leaves from perennial Plants
<p>Freezing data</p>
Data from: Coffee berry borer (Hypothenemus hampei) (Coleoptera: Curculionidae) development across an elevational gradient on Hawai'i Island: applying laboratory degree-day predictions to natural field populations
Coffee berry borer (CBB, Hypothenemus hampei) (Coleoptera: Curculionidae: Scolytinae) is the most destructive pest of coffee worldwide. Information on CBB development times can be used to predict the initiation of new infestation cycles early in the coffee-growing season and thus inform the timing of insecticide applications. While laboratory estimates of CBB development under constant conditions exist, they have not been applied under the heterogeneous environmental conditions that characterize many coffee-growing regions. We measured CBB development times and abundance in commercial coffee farms across an elevational gradient on Hawai'i Island and applied thermal accumulation models from previous laboratory studies to test their fit to field data. Artificial lures were used to infest coffee berries at five farms ranging in elevation from 279-792 m, and weather variables were monitored at macro (farm-level) and micro (branch-level) scales. CBB development was followed in the field from the time of initial berry infestation by the founding female through the development of F1 mature adults. Mean development time from egg to adult across all sites was 38.5 ± 3.46 days, while the mean time required for the completion of a full life cycle (from time of infestation to presence of mature F1 females) was 50.9 ± 3.35 days. Development time increased with increasing elevation and decreasing temperature. Using macro-scale temperature data and two different estimates for the lower temperature threshold (14.9°C and 13.9°C), we estimated a mean requirement of 332 ± 14 degree-days and 386 ± 16 degree-days, respectively, from the time of berry infestation to the initiation of a new reproductive cycle in mature coffee berries. Similar estimates were obtained using micro-scale temperature data, indicating that macro-scale temperature monitoring is sufficient for life-cycle prediction. We also present a model relating elevation to number of CBB generations per month. Our findings suggest that CBB development times from laboratory studies are generally applicable to field conditions on Hawai'i Island and can be used as a decision support tool to improve IPM strategies for this worldwide pest of coffee.
FIGURE 1. Physalis victoriana. A. Habit. B. Flower. C. Extended corolla. D. Gynoecium. E. Flowering calyx. F. Berry and open fruiting calyx. G in Physalis victoriana (Solanaceae) a new species from Northern Argentina
FIGURE 1. Physalis victoriana. A. Habit. B. Flower. C. Extended corolla. D. Gynoecium. E. Flowering calyx. F. Berry and open fruiting calyx. G. Simple, curved, antrorse trichome. H. Glandular short trichome. I. Glandular trichome of the inner face of the fruiting calyx. Drawn from Toledo 1675 by S. Montecchiesi.
Fig. 1 in First Record of the Coffee Berry Borer, Hypothenemus hampei (Ferrari) (Coleoptera: Curculionidae: Scolytinae) on Hainan Island, China
Fig. 1. Coffee berry borer, Hypothenemus hampei, infesting coffee on Hainan Island, China. A) Female, B) Male, C) Infestation on fresh coffee berry, D) Infestation on old and dry coffee berry, E) Beetle gallery in the coffee bean, F) Gallery and adult. Scale in A–B: 1 mm.
FIGURE 4. Philodendron appendiculatum. A. Habit. B. Leaf shape. C. Inflorescence detail. D. Berries. E–J Philodendron cordatum. E. Habit. F in Araceae from Serra do Brigadeiro State Park, Minas Gerais, Brazil
FIGURE 4. Philodendron appendiculatum. A. Habit. B. Leaf shape. C. Inflorescence detail. D. Berries. E–J Philodendron cordatum. E. Habit. F. Leaf shape, detailed inflorescence, berries. G. Stem. H. Inflorescence. I. Spathe detail. J. Berries.
FIGURE 3. Anthurium longifolium. A. Habit. B. Inflorescence before anthesis. C. Berries. Anthurium lucioi. D. Habit. E in Araceae from Serra do Brigadeiro State Park, Minas Gerais, Brazil
FIGURE 3. Anthurium longifolium. A. Habit. B. Inflorescence before anthesis. C. Berries. Anthurium lucioi. D. Habit. E. Leaf shape and inflorescence in anthesis. F. Inflorescence after anthesis. Asterostigma lombardii. G. Habit. H. Leaf shape. I. Inflorescence.
FIGURE 2. Anthurium atrovinosum. A. Habit. B. Inflorescence before anthesis. C. Berries. Anthurium brigadeiroense. D. Inflorescence after anthesis. E. Berries. Anthurium fontellanum. F. Population. G. Habit. H. Leaf shape. I in Araceae from Serra do Brigadeiro State Park, Minas Gerais, Brazil
FIGURE 2. Anthurium atrovinosum. A. Habit. B. Inflorescence before anthesis. C. Berries. Anthurium brigadeiroense. D. Inflorescence after anthesis. E. Berries. Anthurium fontellanum. F. Population. G. Habit. H. Leaf shape. I. Inflorescence in anthesis. Anthurium gladiifolium J. Inflorescence in anthesis. Anthurium scandens subsp. scandens K. Habit and berries.
Fig. 4 in Effect of ozone treatment on glutathione (GSH) status in selected berry fruit
Fig. 4. The effect of ozone treatment on the antiradical activity (A) and H2O2 level (B) in selected berries. Mean values (n = 18) with standard deviation (error bars) with *, **, *** are statistically different from the respective control at p <0.05, p <0.01, and p <0.001, respectively (one-way ANOVA, Tukey test). Mean values with the same lower (control fruit) or upper (ozonated fruit) case are not statistically significant according to the t-Tukey test (p> 0.05). On the figure: ns - not significant.
Fig. 3 in Effect of ozone treatment on glutathione (GSH) status in selected berry fruit
Fig. 3. The effect of ozone treatment ATP level (A) and SDH activity in mitochondria (B) in selected berries. Mean values (n = 18) with standard deviation (error bars) with *, **, *** are statistically different from the respective control at p <0.05, p <0.01, and p <0.001, respectively (one-way ANOVA, Tukey test). Mean values with the same lower (control fruit) or upper (ozonated fruit) case are not statistically significant according to the t-Tukey test (p> 0.05). On the figure: ns - not significant.
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.