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.
91,407
datasets available to search
ShareScore release 0.9.0
Dataset results
91,407 results for “Effectiveness”
Fig. 2 in Effects of Farming Systems on Insect Communities in the Paddy Fields of a Simplified Landscape During a Pest-control Intervention.
Fig. 2. Two-dimensional NMDS ordination of 40 insect communities sampled under different farming systems in northern Taiwan (stress = 0.18).
Fig. 2. Maximum likelihood tree for Crematogaster rothneyi and C. yaharai inferred from 12S in Fig. 7 in Effect of Kleptoparasitic Ants on the Foraging Behavior of a Social Spider ( Karsch, 1891).
Fig. 2. Maximum likelihood tree for Crematogaster rothneyi and C. yaharai inferred from 12S rRNA sequences (12S, 387 bp). Numbers above nodes indicate the bootstrap values. Please note, only one sequence from each population was available.
Fig. 3 in Fig. 7 in Effect of Kleptoparasitic Ants on the Foraging Behavior of a Social Spider ( Karsch, 1891).
Fig. 3. Crematogaster rothneyi. (A, B, C) non-type worker from Calcutta, India (HW 0.8; WL 0.9). (A) body in lateral view; (B) full-face view of head; (C) dorsal view of mesosoma, petiole and postpetiole. (D, E, F) non-type worker from Sulawesi, Indonesia (HW 0.74; WL 0.88). (D) body in lateral view; (E) full-face view of head; (F) dorsal view of mesosoma, petiole and postpetiole.
Fig. 1 in Fig. 7 in Effect of Kleptoparasitic Ants on the Foraging Behavior of a Social Spider ( Karsch, 1891).
Fig. 1. Distribution map of the Crematogaster rothneyi group. Closed circle indicates C. rothneyi, closed triangle indicates C. rothneyi haputalensis, closed square indicates C. yaharai.
Fig. 5 in Fig. 7 in Effect of Kleptoparasitic Ants on the Foraging Behavior of a Social Spider ( Karsch, 1891).
Fig. 5. Left antenna. (A) Crematogaster rothneyi; (B) Crematogaster yaharai. Arrow indicates antennal segments V and VI.
Fig. 4 in Fig. 7 in Effect of Kleptoparasitic Ants on the Foraging Behavior of a Social Spider ( Karsch, 1891).
Fig. 4. Crematogaster yaharai, paratype worker from Cambodia (HW 0.72; WL 0.83). (A) body in lateral view; (B) full-face view of head; (C) dorsal view of mesosoma, petiole and postpetiole.
Fig. 7 in Effect of Kleptoparasitic Ants on the Foraging Behavior of a Social Spider ( Karsch, 1891).
Fig. 7. Handling time (minutes) of both K unexposed (Ku, n = 3 groups) and K exposed (Ke, n = 3 groups) spider groups recorded during three different times (9 am, 1 pm and 5 pm) of the four experimental days.
Fig. 4 in Effect of Kleptoparasitic Ants on the Foraging Behavior of a Social Spider ( Karsch, 1891).
Fig. 4. Web rebuilding ability (Size of the web (cm2 ± SEM) of the K unexposed (Kleptoparasite "K" is O. smaragdina) spider groups (Fasted (n = 3 groups) and Fed (n = 3 groups)) during the 4 experimental days. The regression lines, blue line (Fasted spider) has the Intercept a = 236.94, Slope b = 71.812 and Coefficient of Determination R² = 0.966 and the red line (Fed spider) has a = 78.925, b = 55.61 and R² = 0.955.
Fig. 3 in Effect of Kleptoparasitic Ants on the Foraging Behavior of a Social Spider ( Karsch, 1891).
Fig. 3. Kleptoparasites of S. sarasinorum. (A) Argyrodes kumadai (Dewdrop spider). (B) Hyllus semicupreus (Heavy-bodied jumper). (C) Phintella vittata (Banded phintella). (D) Oxyopes javanus (Lynx spider). (E) Oecophylla smaragdina (Weaver ant). (F) Anoplolepis gracilipes (Yellow crazy ant). Photo courtesy of: Karunnappilli S. Nafin.
Fig. 6 in Effect of Kleptoparasitic Ants on the Foraging Behavior of a Social Spider ( Karsch, 1891).
Fig. 6. Size of the web (cm2 ± SEM) built by fed and fasted (K unexposed ("- K exposure"): n = 3 groups) and K exposed ("+ K exposure"): n = 3 groups) spider groups.
Fig. 2 in Effect of Kleptoparasitic Ants on the Foraging Behavior of a Social Spider ( Karsch, 1891).
Fig. 2. (A) An individual colony of S. sarasinorum. (B) Experimental set-up for the study. (C) Spiders (Host) in captivity- Ant (Kleptoparasite- O. smaragdina) exposed.
Fig. 5 in Effect of Kleptoparasitic Ants on the Foraging Behavior of a Social Spider ( Karsch, 1891).
Fig. 5. Web rebuilding ability (Size of the web (cm2 ± SEM)) of the K exposed (Kleptoparasite "K" is O. smaragdina) spider groups (Fasted (n = 3 groups) and Fed (n = 3 groups)) during the 4 experimental days. The regression lines, blue line (Fasted spider) has the Intercept a = 64.13, Slope b = 73.361 and Coefficient of Determination R2 = 0.96 and the red line (Fed spider) has a = 41.5, b = 65.25 and R2 = 0.948.
Fig. 1 in Effect of Kleptoparasitic Ants on the Foraging Behavior of a Social Spider ( Karsch, 1891).
Fig. 1. Map of the study area – Social spider web colonies (Marked as red spot) on Christ College Irinjalakuda.
dataset: The Effects of Density on the Growth and Temperature Production of Tenebrio molitor Larvae
Open the record for dataset details and reuse information.
Fig. 1 in Manifold habitat effects on the prevalence and diversity of avian blood parasites
Fig. 1. Diagram illustrating how conditions of the vector, parasite, host and habitat must all be permissive for pathogen transmission to occur. The outer layer depicts some factors that are currently causing rapid environmental change, which will affect host‾parasite dynamics.
Fig. 6 in Climate change, biodiversity, ticks and tick-borne diseases: The butterfly effect
Fig. 6. Podolica cattle in the Gallipoli Cognato Regional Park, Basilicata, southern Italy. These cattle move freely within the park's territory, helping in disseminating Ixodes ricinus to different altitudes (from 200 m to over 1000 m).
Fig. 5. A in Climate change, biodiversity, ticks and tick-borne diseases: The butterfly effect
Fig. 5. A male of the winter tick Haemaphysalis inermis collected in a cold winter day in January 2010 in Basilicata, southern Italy.
Fig. 4 in Climate change, biodiversity, ticks and tick-borne diseases: The butterfly effect
Fig. 4. Shanghai, China: the largest city proper by population in the world. China is the world's largest carbon emitter; it accounted for 29% of global total emissions in 2012 (Olivier et al., 2013).
Fig. 3 in Climate change, biodiversity, ticks and tick-borne diseases: The butterfly effect
Fig. 3. Deforestation of Atlantic rainforest for the establishment of banana tree plantations in Amaraji, north-eastern Brazil.
Fig. 1 in Climate change, biodiversity, ticks and tick-borne diseases: The butterfly effect
Fig. 1. Climate change is contributing to sea level rise. The Boa Viagem beach is a tourist destination in Recife, north-eastern Brazil. If current trends in sea level rise persist, cities like Recife may be literally swallowed the sea in the coming decades.
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.