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.
1,425
datasets available to search
ShareScore release 0.7.1
Dataset results
1,425 results for “Agriculture”
Fig. 5 in Fig. 13 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.
Fig. 5. The coloration of Parasesarma liho in the field in Taiwan. A, specimen (not captured) from Gangkou R. estuary, Pingtung; B, specimen (not captured) from Meilun R. estuary, Hualien.
Fig. 2 in Fig. 13 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.
Fig. 2. The morphological variation of distal part the right G1s of Parasesarma liho (A–H), and P. paucitorum (I). A, CW 11.1 mm (NCHUZOOL 15022), Pingtung, Taiwan; B, CW 11.6 mm (NCHUZOOL 15027), Hualien, Taiwan; C, CW 12.7 mm (ZSM A20100040, paratype of P. liho), Hualien, Taiwan; D, CW 13.29 mm (NCHUZOOL 15034), Cebu, Philippines; E, CW 14.3 mm (NMMBCD 3975, holotype of P. cognatum), Pingtung, Taiwan; F, CW 15.5 mm (ZRC 2019.0578, paratype of P. paucitorum), Sulawesi, Indonesia; G, CW 16.2 mm (NCHUZOOL 15022), Pingtung, Taiwan; H, CW 16.7 mm (NCHUZOOL 15031), Pingtung, Taiwan; I, CW 19.7 mm (MZB Cru 2243, holotype of P. paucitorum), Sulawesi, Indonesia. Scales bars = 0.5 mm.
Fig. 5 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.
Fig. 5. Relationship between species abundance and climatic predictors according to the generalized linear models. Solid lines represent the fitted values (prediction) of the models, and the shaded area shows the 95% confidence interval of the predicted values of each model. Colour-code points indicate data by precipitation season (low and high).
Fig. 1 in Fig. 13 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.
Fig. 1. Schematic drawing showing the measurement of the length, as well as the maximum and minimum widths of the propodi of the fourth pereiopods (third ambulatory leg, P4) used in this study.
Fig. 3 in Fig. 3 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.
Fig. 3. Schematic diagram of bird hatchlings. Dorsal (upper row) and ventral (lower row) views of chicken (precocial), pigeon (semialtricial), parrot (altricial) and zebra finch.
Fig. 1 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.
Fig. 1. Geographic location of the study area in relation to South America (A), Venezuela (B), Mérida State (C), and the Monte Zerpa Cloud Forest (D). Points indicate sampled areas.
Fig. 3 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.
Fig. 3. Seasonal climatic and anuran variation among sampling sessions. (A) Principal Component Analysis (PCA) for all individual climate variables measured in 24 sampling sessions. The analysis included precipitation (Pp), relative humidity (RH) and air temperature (Temp). The level of Pearson correlation of each vector is indicated (cos2). (B) Principal Coordinate Analysis (PCoA) for the anuran assemblage based on species composition and abundance during the high and low precipitation seasons. The centroid points represent the average precipitation each month.
Fig. 2 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.
Fig. 2. Anuran species recorded in the Monte Zerpa Cloud Forest. Hyalinobatrachium duranti (A), Hyloscirtus platydactylus (B), Hyloscirtus jahni (C), and Pristimantis vanadisae (D). Photos: Francisco Nava (A, C, D) and Pascual Soriano (B).
Fig. 2 in Fig. 3 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.
Fig. 2. Schematic diagram of feather tract and types of natal down formation in zebra finch and chicken. Zebra finch embryos show two types of feather formation: Type I feather formation (open circles), in which the feather buds do not develop into downy feather; Type II feather formation (black circles), in which the feather buds develop into downy feathers, which are later replaced by contour feathers. Chicken embryos exhibit only the Type II feather formation. E8, E9, and E12: embryo day 8, 9 and 12, respectively. D7: 7 days post-hatch. Scale bar = 0.1 cm. The figure was modified from our previous study (Chen et al. 2017).
Fig. 4 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.
Fig. 4. Abundance variation of anurans in the Monte Zerpa Cloud Forest. Differences in overall abundances among species (A), total anuran abundance between precipitation seasons (B), abundances by species between seasons (C) are presented. Letters indicate significant differences among groups according to post hoc tests (p <0.05), while ns indicates non-significant differences between samples.
Fig. 7 in Fig. 13 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.
Fig. 7. Genealogical network for the COI haplotypes observed within the clades of Parasesarma liho and other related species. Unlabelled hatches indicate inferred haplotypes not found in the sampled population. For haplotype names, see table 1.
Fig. 1. The modified time calibrated Bayesian tree and a in Fig. 3 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.
Fig. 1. The modified time calibrated Bayesian tree and a plot of four major avian developmental modes (Prum et al. 2015). The complete tree is divided into parts A and B. Scale in the Y-axis: millions of years ago.
Fig. 4 in Fig. 13 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.
Fig. 4. The outer surface of chelipedal meri of Parasesarma cognatum (holotype, NMMBCD 3975). A, left cheliped; B, right cheliped. Arrow indicates a subdistal angle on the upper margin of chelipedal merus.
Fig. 6. A in Fig. 13 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.
Fig. 6. A Bayesian inference (BI) tree of Parasesarma liho, as well as the outgroups, based on the cytochrome oxidase subunit I genes (COI). Probability values at the nodes represent support values for BI and maximum likelihood (ML). For haplotype names, see table 1.
Fig. 3 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.
Fig. 3. The relationship between nesting CCL (curved carapace lenght) size and latitude in marine turtles across different regions.
Fig. 2 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.
Fig. 2. The temporal change in the CCL (curved carapace length) and CCW (curved carapace width) values over the years (Black lines are Theil-Sen trend lines).
Fig. 12. A in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.
Fig. 12. A Bayesian inference tree of the Austruca variegata complex, with the outgroups of other congeneric species, based on the combined 28S, 16S and COI markers. Values at the nodes are Bayesian posterior probabilities.
Fig. 13 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.
Fig. 13. Genealogical network for the COI haplotypes observed within the clades of Austruca variegata (Heller, 1862), A. bengali (Crane, 1975) and A. triangularis (A. Milne-Edwards, 1873). Unlabelled hatches indicate inferred haplotypes not found in the sampled population. For haplotype names, see table 1.
Fig. 2 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.
Fig. 2. Austruca variegata (Heller, 1862). a–d, male (CW 18.6 mm, CL 10.7 mm, PL 26.6 mm, ZRC 2018.1375). (a) habitus; (b) major cheliped; (c) pleon; (d) minor cheliped. Scale bar = 5.0 mm.
Fig. 8 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.
Fig. 8. Female Austruca variegata (Heller, 1862) (a–d), A. bengali (Crane, 1975) (e) and A. triangularis (A. Milne-Edwards, 1873) (f). (a) habitus; (b) floor of right orbit; (c) right minor cheliped; (d–f) right vulva (gonopore). (a–d) CW 16.6 mm (NCHUZOOL 14365; Tamil Nadu, India); (e) CW 12.4 mm (QM W27320; Phuket, Thailand); (f) CW 14.6 mm (NCHUZOOL 14350; Cebu, Philippines). Scale bars: b, c = 5.0 mm, d–f = 0.5 mm
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.