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Figure 2 in Effect of Pupal Holding Density on Emergence Rate, Flight Ability, and Yield of Sterile Male Mediterranean Fruit Flies (Diptera: Tephritidae)
Figure 2. Estimated numbers of fliers produced per tower (top) and ratios of number of fliers produced to number of pupae placed per tower (bottom) in relation to the pupal loading level per constituent tray. Hawaii-derived flies were used exclusively; towers contained 52 trays. Symbols represent means over 33 towers per loading level (3 towers per test day x 11 test days); error bars represent ± 1 SE.
Fig. 1 in It is recreational but profitability also matters: A cost-effective economic approach to marine recreational fishing in Spain Abstract
Fig. 1: Map of the study area. The darker regions highlighted correspond to Spanish coastal Autonomous Communities.
Fig. 4 in It is recreational but profitability also matters: A cost-effective economic approach to marine recreational fishing in Spain Abstract
Fig. 4: Economic indicator by: A) the main fishing modalities: spearfishing, shore-fishing and boat-fishing and B) spearfishing diving approach.
Fig. 3 in It is recreational but profitability also matters: A cost-effective economic approach to marine recreational fishing in Spain Abstract
Fig. 3: Daily expenses. A) Spearfishing by diving approach and B) Boat fishing (angling) by type of vessel. The percentage of responses by modality in brackets.
Fig. 6 in Effect of Nutrient, Light Intensity and Temperature on the Growth Rates and Metabolism of a Stress-Resistant Bacillariophyta Species Entomoneis sp. - in Izmir Bay (Aegean Sea) Abstract
Fig. 6: Maxiumum growth rate determination of all temperatures, light intensities and nutrient concentrations.
Fig. 5 in Effect of Nutrient, Light Intensity and Temperature on the Growth Rates and Metabolism of a Stress-Resistant Bacillariophyta Species Entomoneis sp. - in Izmir Bay (Aegean Sea) Abstract
Fig. 5: Entomoneis sp biomass (Chl a, µg /L) under different N/P ratios and light intensities (a) representing growth under T1°C (b) T2°C (c) and T3°C.
Fig. 2 in Effect of Nutrient, Light Intensity and Temperature on the Growth Rates and Metabolism of a Stress-Resistant Bacillariophyta Species Entomoneis sp. - in Izmir Bay (Aegean Sea) Abstract
Fig. 2: 3D response surface plot and contour line of Box– Behnken Design showing the mutual effect of temperature and light intensity on chlorophyll a concentration (µg/L) of Entomoneis sp. using an N/P ratio of 11.
Fig. 3 in Effect of Nutrient, Light Intensity and Temperature on the Growth Rates and Metabolism of a Stress-Resistant Bacillariophyta Species Entomoneis sp. - in Izmir Bay (Aegean Sea) Abstract
Fig. 3: 3D response surface plot and contour line of Box– Behnken Design showing the mutual effect of temperature and light intensity on growth rate (day-1) of Entomoneis sp. using an N/P ratio of 4.4.
Fig. 4 in Effect of Nutrient, Light Intensity and Temperature on the Growth Rates and Metabolism of a Stress-Resistant Bacillariophyta Species Entomoneis sp. - in Izmir Bay (Aegean Sea) Abstract
Fig. 4: 3D response surface plot and contour line of Box– Behnken Design showing the mutual effect of temperature and light intensity on growth rate (day-1) of Entomoneis sp. using an N/P ratio of 27.
Fig. 5 in Fish assemblages along the coasts of Tunisia: a baseline study to assess the effectiveness of future Marine Protected Areas
Fig. 5: Size-class (S: small, M: medium and L: large) frequency distribution (%) of relevant target fishes in Unprotected (UP) and Future Protected (FP) zones at the three studied locations (KU: Kuriat Islands, CNCS: Cap Negro-Cap Serrat, TA: Tabarka), (Number of individuals used to calculate percentages is given in Supp. Mat. 2).
Fig. 3 in Fish assemblages along the coasts of Tunisia: a baseline study to assess the effectiveness of future Marine Protected Areas
Fig. 3: Mean density (±standard error) per trophic category at the sampling locations (KU: Kuriat Islands, CNCS: Cap Negro-Cap Serrat, TA: Tabarka) and per protection level (UP: Unprotected, FP: Future Protected).
Fig. 1 in Fish assemblages along the coasts of Tunisia: a baseline study to assess the effectiveness of future Marine Protected Areas
Fig. 1: Locations where MPAs will be established along the Tunisian coast. Location of future protected sites (FP) and those outside (that will remain unprotected) (UP) (separated with dotted lines indicating borders of future MPAs as they are proposed in management plans).
Fig. 4 in Fish assemblages along the coasts of Tunisia: a baseline study to assess the effectiveness of future Marine Protected Areas
Fig. 4: Mean biomass (±standard error) per trophic category at the sampling locations (KU: Kuriat Islands, CNCS: Cap Negro-Cap Serrat, TA: Tabarka) and per protection level (UP: Unprotected, FP: Future Protected).
Fig. 2 in Fish assemblages along the coasts of Tunisia: a baseline study to assess the effectiveness of future Marine Protected Areas
Fig. 2: Mean species richness (a), mean density (b) and mean biomass (c) (±standard error) per location (KU: Kuriat islands, CNCS: Cap Negro-Cap Serrat, TA: Tabarka) and protection level (UP: Unprotected, FP: Future Protected).
Figure 3 in Mowing inhibits the invasion of the alien species Solidago altissima and is an effective management strategy
Figure 3. (a) Aboveground biomass of S. altissima in September 2019. (b) Biomass of rhizomes of S. altissima in September 2019. Mowing 1: mowed once in July; Mowing 2: mowed twice in May and September; Mowing 3: mowed three times in May, July, and September. Data are presented as means ± standard errors of 14 replicates. Bars with different letters are significantly different at p <0.05 (ANOVA with post hoc Tukey's test).
Figure 4 in Mowing inhibits the invasion of the alien species Solidago altissima and is an effective management strategy
Figure 4. Effects of control practices on flowering rates of S. altissima in October 2019. Mowing 1: mowed once in July; Mowing 2: mowed twice in May and September; Mowing 3: mowed three times in May, July, and September. Data are presented as means ± standard errors of 14 replicates. Bars with different letters are significantly different at p <0.05 (ANOVA with post hoc Tukey's test).
Figure 2 in Variation in glyphosate effects and accumulation in emergent macrophytes
Figure 2. Concentration-response relationships for Phragmites australis (top graph), Typha latifolia (middle graph) and Typha × glauca (bottom graph) based on the proportion of dead shoots observed 27 days post-exposure to 0–8% glyphosate (Roundup WeatherMAX® formulation). Each treatment was replicated seven times per taxa, except T. latifolia at 5% (n = 6). Measured concentrations were used for modelling (Table S2). Grey points represent the replicates and are darker when points overlap; grey shading illustrates the 95% confidence bounds of the concentration-response model; solid red dots represent LC50 estimates; LC50 estimates on top left corner of each graph are given with lower and upper 95% confidence limits.
Figure 3 in Variation in glyphosate effects and accumulation in emergent macrophytes
Figure 3. Average residues of glyphosate (left) and aminomethylphosphonic acid (AMPA; right) detected in above-ground plant tissues of the three macrophytes Phragmites australis (PA), Typha latifolia (TL) and Typha × glauca (TXG) 27 days post-exposure to 8% and 5% glyphosate solutions (Roundup WeatherMAX® formulation). Four replicates per taxon and treatment, except for TL at 5% (n = 3); error bars represent standard errors of the means; letters a-b (left plot) and c-d (right plot) indicate significant differences in residues among taxa. Note y-axes have different scales.
Figure 1 in Mowing inhibits the invasion of the alien species Solidago altissima and is an effective management strategy
Figure 1. (a) Coverage of S. altissima and (b) the average number of species per quadrat in the S. altissima-dominant areas or uninvaded areas. Data are presented as means ± standard errors of 14 replicates. Bars with different letters are significantly different at p <0.05 (Student's t-test).
Figure 2 in Mowing inhibits the invasion of the alien species Solidago altissima and is an effective management strategy
Figure 2. Number of shoots of S. altissima in March 2018 and April 2019. Mowing 1: mowed once in July; Mowing 2: mowed twice in May and September; Mowing 3: mowed three times in May, July, and September; Eco 200: 30% of shoots in the quadrats were cut near the ground, and the cut surfaces were covered with Eco 200 block. Data are presented as means ± standard errors of 14 replicates. Bars with different letters are significantly different at p <0.05 (ANOVA with post hoc Tukey's test).
ScienceDex guides
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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.