Find research datasets worth reusing

opencc-by-4.0Oct 2018View details →

Less is More: Exploiting the Standard Compiler Optimization Levels for Better Performance and Energy Consumption

The data used to generate the graphs in Figures 2 and 3 of the paper "Less is More: Exploiting the Standard Compiler Optimization Levels for Better Performance and Energy Consumption" at SCOPES'18. The data includes power consumption, code size, and running time, indexed by an ID that identifies the combination of compiler options. Data is stored in a CSV file that identifies the specific benchmark, organized into a zip file that identifies the chip architecture. See README.txt for details.

opencc-by-4.0Mar 2014View details →

Figure 3 in Reproductive cycle of the traditionally exploited sea cucumber Holothuria tubulosa (Holothuroidea: Aspidochirotida) in Pagasitikos Gulf, western Aegean Sea, Greece

Figure 3. Temporal allocation of the developmental stages in males and females of H. tubulosa at Pagasitikos Gulf. I, recovery stage; II, growing; III, mature; IV, spawning; V, postspawning.

opencc-by-4.0Dec 2012View details →

Figure 4. Xylosandrus compactus boring coffee berries around the blossom area. X. compactus boring a in First Report of Exploitation of Coffee Beans by Black Twig Borer (Xylosandrus Compactus) and Tropical Nut Borer (Hypothenemus obscurus) (Coleoptera; Curculionidae: Scolytinae) in Hawaii

Figure 4. Xylosandrus compactus boring coffee berries around the blossom area. X. compactus boring a coffee berry (A, left), hole made by X. compactus on the endosperm (B, right); galleries or immature stages were not found.

opencc-by-4.0Dec 2012View details →

Figure 2 in First Report of Exploitation of Coffee Beans by Black Twig Borer (Xylosandrus Compactus) and Tropical Nut Borer (Hypothenemus obscurus) (Coleoptera; Curculionidae: Scolytinae) in Hawaii

Figure 2. Gallery of Xylosandrus compactus in coffee branches. Xylosandrus compactus female adults (left) and immature stages (right).

opencc-by-4.0Dec 2012View details →

Figure 3 in First Report of Exploitation of Coffee Beans by Black Twig Borer (Xylosandrus Compactus) and Tropical Nut Borer (Hypothenemus obscurus) (Coleoptera; Curculionidae: Scolytinae) in Hawaii

Figure 3. Damage symptoms of X. compactus in coffee branches. First leaves turn light green (A, left), then the wilted leaves and bark beyond the affected area turn brown or black (B, right).

opencc-by-4.0Dec 2023View details →

Global gridded fishing exploitation patterns (F/FMSY) of demersal and pelagic fish

Global gridded fishing mortality (F) relative to the fishing mortality that supports maximum sustainable yield (FMSY) for three fish functional types: forage fish, large pelagic fish, and demersal fish.  <ul> <li>Years 1841-2004</li> <li>0.5-degree spatial resolution</li> </ul> Outputs can be used to simulate historical fishing patterns of pelagic and demersal fish in ecosystem models. The F/FMSY needs to be multiplied with FMSY of each fish type in the model to obtain F. FMSY will depend on fish model specification and assumptions. Outputs are also provided as a time series per functional type and LME. The F/FMSY timeseries are estimated using reconstructed catch data and a data limited catch assessment model for all LME × functional type combinations with intermediate and high catches. For all remaining combinations and the high seas, F/FMSY timeseries are estimated by converting nominal effort timeseries per functional type to an F/FMSY using conversion factors. The estimated F/FMSY timeseries are allocated per functional type, ecosystem, and year across a 0.5-degree spatial grid in proportion to total gridded effort in each ecosystem. The gridded F/FMSY are used as input into the FEISTY model forced by outputs from GFDL’s ocean model (MOM6-COBALTv2) to generate historical time series of fish biomass and catch. The catch and biomass simulated FEISTY outputs are available between 1961 and 2004 for each LME and the High seas.  Reference to the paper with full description of the analysis:  <ul> <li>van Denderen PD, N Jacobsen, KH Andersen, JL Blanchard, C Novaglio, CA Stock, CM Petrik (submitted) Estimating fishing exploitation rates to simulate global catches and biomass changes of pelagic and demersal fish Earth's Future </li> </ul> Additional data sources: <ul> <li>Reconstructed fisheries catches: Watson, R. A database of global marine commercial, small-scale, illegal and unreported fisheries catch 1950–2014. Sci Data 4, 170039 (2017). <a href="https://doi.org/10.1038/sdata.2017.39">https://doi.org/10.1038/sdata.2017.39</a></li> <li>Novaglio, C., Rousseau, Y., Watson, R. A., & Blanchard J. L. (2024). ISIMIP3a reconstructed fishing activity data (v1.0) [data set]. ISIMIP Repository. <a href="https://doi.org/10.48364/ISIMIP.240282">https://doi.org/10.48364/ISIMIP.240282</a></li> <li>Global gridded fishing effort data reconstruction: Rousseau, Y., Blanchard, J. L., Novaglio, C., Pinnell, K., Tittensor, D. P., Watson, R. A., & Ye, Y. (2022). Global Fishing Effort [Data]. Institute for Marine and Antarctic Studies (IMAS), University of Tasmania (UTAS).</li> </ul>

opencc-by-4.0Oct 2024View details →

City's Low Hanging Fruit: Exploring Policy Alternatives for Exploiting Urban Fruit Trees

City's Low Hanging fruit: Map, Thematic analysis, Three quistionnaires, questionnaire answers מפה, ניתוח תמטי, שלושת השאלונים, תשובות לשאלונים Abstract + methods - below תקציר - למטה

FIG. 14 in The modus operandi of walrus exploitation during the Palaeoeskimo period at the Tayara site, Arctic Canada

FIG. 14. — Typology of the harpoon heads found in Level II of the Tayara site (Taylor 1968; Houmard 2011a, 2011b).

FIG. 9 in The modus operandi of walrus exploitation during the Palaeoeskimo period at the Tayara site, Arctic Canada

FIG. 9. — Anterior view of walrus skull showing grooving longitudinally and transversely for tusk extraction: A, drawing after LeMoine & Darwent 1998: 77; B, Tayara fragment (AD 202-444).

FIG. 8 in The modus operandi of walrus exploitation during the Palaeoeskimo period at the Tayara site, Arctic Canada

FIG. 8. — Evidence of use-wear of initial processing of carcasses and skin treatment: A, chert scraper used to softened the skin, as shown by the mat and dense polish with perpendicular orientation from the edge, and the rounfding of the edge (100x); B, Chert microblade used to skinning a caracasses or defleshing a fresh skin as shown by the diffused polish mixed with oblique scars along the edge (100x); C, Quartz microblades used as a burin, to engrave a hard and dry material like bone or ivory, as shown by the abraded area, linear and discontinouous, observed on the modidied part of the edge (400x).

FIG. 6 in The modus operandi of walrus exploitation during the Palaeoeskimo period at the Tayara site, Arctic Canada

FIG. 6. Diagrammatic representation of walrus butchering, Southampton Island in 1970 (After Freeman 1974/75: 151; A, very large adult; B, adult; C, immature or adult; D, E, immature; F, immature and calf).

FIG. 5 in The modus operandi of walrus exploitation during the Palaeoeskimo period at the Tayara site, Arctic Canada

FIG. 5. — Distal fragment of a biface end blade embedded in the rib of a walrus (Drawing P. M. Desrosiers).

FIG. 3 in The modus operandi of walrus exploitation during the Palaeoeskimo period at the Tayara site, Arctic Canada

FIG. 3. — Skeletal profile of the walrus in Level II based on percentage of survival (MNI = 6, data from Table 2). (Drawing Michel Cou- tureau, available in http:www.archeozoo.org).

FIG. 4 in The modus operandi of walrus exploitation during the Palaeoeskimo period at the Tayara site, Arctic Canada

FIG. 4. — Diagram of the maximum length (mm) and the maximum height (mm) and mixture analysis curve of the maximum length of the Tayara and Foxe Basin walrus mandibles (reference collection: Stewart, personal data in Wiig et al., 2007). (Mixture analysis, Cutoff point = 235.277 after Monchot & Léchelle 2002).

FIG. 2 in The modus operandi of walrus exploitation during the Palaeoeskimo period at the Tayara site, Arctic Canada

FIG. 2. — Distribution of worked artefacts by raw material and species, quantified by number of specimens

Figure 4 in Exploiting assembly pheromone for the control of ixodid ticks

Figure 4 Comparison of the per cent death of adult ticks after 1 hour in Assembly pheromonedeltamethrin and deltamethrin treatment.

Figure 3 in Exploiting assembly pheromone for the control of ixodid ticks

Figure 3 Comparison of the per cent death of ixodid tick larvae after 1 hour in Assembly pheromonedeltamethrin and deltamethrin treatment.

Figure 2 in Exploiting assembly pheromone for the control of ixodid ticks

Figure 2 Behavioural responses of ixodid tick larvae to assembly pheromone: A – Curled leg appearance ofHyalomma marginatumlarvae; B

Figure 1 in Exploiting assembly pheromone for the control of ixodid ticks

Figure 1 Effect of assembly pheromone: A – Clustering ofRhipicephalus sanguineuslarvae on assembly pheromone impregnated filter paper disc; B –Arrestment of Rhipicephalus sanguineus larvae on assembly pheromone impregnated filter paper disc; C – Behaviour of the adults of Rhipicephalus sanguineus in assembly pheromone-deltamethrin trial; D – Behaviour of the adults ofRhipicephalus sanguineusin positive control; E – Behaviour of the adults ofRhipicephalus sanguineusin negative control; F – Response of the adults ofRhipicephalus sanguineus to natural assembly pheromone.