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Figure5 in Habitat-Based Breeding Strategies of Female Hoplobatrachus occipitalis (Anura: Dicroglossidae) from Daloa Department, Midwest of Côte d'Ivoire
Figure5. Egg diameter frequency distribution of female Hoplobatrachus occipitalis from Fatiga and Zaliohouan in Daloa Department.
Fig 5 in Monitoring Spodoptera frugiperda in Benin: assessing the influence of trap type, pheromone blends, and habitat on pheromone trapping
Fig 5. Phylogenetic tree based on a portion of the COI barcoding segment showing the relationships of selected non-target moth specimens (g54xxx) isolated from fall armyworm pheromone traps relative to selected GenBank sequences. GenBank sequences are indicated by species name followed by accession number. Fall armyworm R-strain and fall armyworm C-strain are consensus sequences for the 2 fall armyworm host strains.
Figure4 in Habitat-Based Breeding Strategies of Female Hoplobatrachus occipitalis (Anura: Dicroglossidae) from Daloa Department, Midwest of Côte d'Ivoire
Figure4. Spatial variability in gonado-somatic index of female Hoplobatrachus occipitalis from Fatiga and Zaliohouan in Daloa Department
Figure3 in Habitat-Based Breeding Strategies of Female Hoplobatrachus occipitalis (Anura: Dicroglossidae) from Daloa Department, Midwest of Côte d'Ivoire
Figure3. Spatial variability in size (SVL) of female Hoplobatrachus occipitalis from Fatiga and Zaliohouan in Daloa Department
Figure8 in Habitat-Based Breeding Strategies of Female Hoplobatrachus occipitalis (Anura: Dicroglossidae) from Daloa Department, Midwest of Côte d'Ivoire
Figure8. Regression between female size (SVL) and egg diameter in Hoplobatrachus occipitalis from Fatiga and Zaliohouan in Daloa Department
Fig 3 in Monitoring Spodoptera frugiperda in Benin: assessing the influence of trap type, pheromone blends, and habitat on pheromone trapping
Fig 3. Field screening of home-made trap design (Jar2 and Jar4) in comparison to Unitrap model using pheromone lures (all combined) over 2 maize cropping systems (maize monoculture and maize-cowpea intercrops) during the second planting season. The traps were installed on 30 Sep 2019 during the second maize growing season, and the moth collection period covered Oct to Dec. The data denotes average numbers per trap type for overall 3-d intervals moth collections with standard errors.
Fig 2 in Monitoring Spodoptera frugiperda in Benin: assessing the influence of trap type, pheromone blends, and habitat on pheromone trapping
Fig 2. Preliminary field test of pheromone traps using the 2-component fall armyworm pheromone PSU lure during the first maize growing season: comparison between home-made Jar2 trap and Unitrap model (A) (average number per trap type for overall weekly moth collections; error bars represent standard error and different lowercase letters denote statistical difference), and fluctuation in moth trap catch of the Unitrap-2-component lure combination (B) (moth collections were done every 3 d).
Fig 4 in Monitoring Spodoptera frugiperda in Benin: assessing the influence of trap type, pheromone blends, and habitat on pheromone trapping
Fig 4. Moth trap catch of 3 pheromone lures over 2 cropping systems (maize monoculture and maize-cowpea intercrops) using Unitraps. The traps were installed on 30 Sep 2019 during the second maize growing season and allowed to collect moths Oct to Dec 2019. The 4-component lure type (4C) contained Z9-14:Ac (78.3%), (Z)-11-hexadecenyl acetate (Z11-16:Ac) (3.6%), Z7-12:Ac (11.2%), and (Z)-9-dodecenyl acetate (Z9-12:Ac) (7.0%); whereas the 3-component lure type (3C) was composed of Z9-14:Ac (66.1%), Z11-16:Ac (4.7%), and Z7-12:Ac (29.3%); and the 2-component lure type (2C) of Z9-14:Ac (90.5%) and Z7-12:Ac (9.5%). The data represents average numbers for overall 3-d intervals moth collections.
Fig 1 in Monitoring Spodoptera frugiperda in Benin: assessing the influence of trap type, pheromone blends, and habitat on pheromone trapping
Fig 1. Traps used in study: commercially available Unitrap (A); home-made Jar2 trap constructed from 2 L plastic jar (B). The Jar2 trap was designed by G.T. TepaYotto and J.K. Winsou.
Fig. 3 in Use of baits for the evaluation of underground termites (Blattodea: Rhinotermitidae) in different habitats of the southern Amazon region
Fig. 3. Queen of Heterotermes tenuis (center circle) in early stage of egg production (circle on lef), and colony formation inside the cardboard bait in southern Amazonia.
Fig 4 in Spatiotemporal distribution of stink bugs (Hemiptera: Pentatomidae) in peach orchards and surrounding habitat
Fig 4. Interpolated maps of Euschistus tristigmus adult distributions in peach orchards and surrounding habitat early season (wk 1), mid-season (wk 8), and late season (wk 12) in 2002 and 2003.
Fig. 2 in Use of baits for the evaluation of underground termites (Blattodea: Rhinotermitidae) in different habitats of the southern Amazon region
Fig. 2. Predominant termites in this study in southern Amazonia: (A) Nasutitermes sp. soldier; (B) Heterotermes tenuis soldier.
Fig. 1 in Use of baits for the evaluation of underground termites (Blattodea: Rhinotermitidae) in different habitats of the southern Amazon region
Fig. 1. Spatial arrangement of Termitrap® baits within plots for subterranean termite survey in different environments in southern Amazonia.
Fig. 2 in Spatiotemporal distribution of stink bugs (Hemiptera: Pentatomidae) in peach orchards and surrounding habitat
Fig. 2. Seasonal capture of Euschistus servus and Euschistus tristigmus in pheromone-baited traps; (A) mean number of E. servus and E. tristigmus per pheromonebaited trap in peach and non-crop habitat over time in 2002; (B) mean number of E. servus and E. tristigmus per pheromone-baited trap in peach and surrounding habitat over time in 2003.
Fig 3 in Spatiotemporal distribution of stink bugs (Hemiptera: Pentatomidae) in peach orchards and surrounding habitat
Fig 3. Interpolated maps of Euschistus servus adult distributions in peach orchards and surrounding non-crop habitat early season (wk 1), mid-season (wk 8), and late season (wk 12) in 2002 and 2003.
Fig. 1 in Spatiotemporal distribution of stink bugs (Hemiptera: Pentatomidae) in peach orchards and surrounding habitat
Fig. 1. Spatiotemporal distribution patterns of Euschistus servus and Euschistus tristigmus: (A) number of traps in which E. servus and E. tristigmus were present in peach and surrounding habitat; (B) number of traps in which stink bugs were present over the season in peach and surrounding habitat.
Fig 4 in First record of Raorchestes longchuanensis Yang and Li, 1978 (Anura: Rhacophoridae) from northeastern Bangladesh suggests wide habitat tolerance
Fig 4. Advertisement call of Raorchestes longchuanensis at ambient air temperature 27.4 °C. (A) A call consists of five call groups, numbers on the top indicate pulse numbers in the respective call group. (B) Spectrogram of the call. (C) First call group with four pulses. (D) A pulse of the 5th call group.
Fig 3 in First record of Raorchestes longchuanensis Yang and Li, 1978 (Anura: Rhacophoridae) from northeastern Bangladesh suggests wide habitat tolerance
Fig 3. Color variation in Raorchestes longchuanensis. (A) Pale brown dorsum with faint ")(" mark; (B) Dark brown dorsum with prominent ")(" mark; (C) Dark chocolate color dorsum without mid-dorsal line; (D) Dark chocolate color dorsal side with narrow yellow mid-dorsal line.
Fig 2 in First record of Raorchestes longchuanensis Yang and Li, 1978 (Anura: Rhacophoridae) from northeastern Bangladesh suggests wide habitat tolerance
Fig 2. Maximum likelihood phylogenetic tree based on 16S rRNA genes, showing the identity of the specimens as Raorchestes longchuanensis. The red box shows the specimens from the present study.
Fig 1 in First record of Raorchestes longchuanensis Yang and Li, 1978 (Anura: Rhacophoridae) from northeastern Bangladesh suggests wide habitat tolerance
Fig 1. External features of Raorchestes longchuanensis. (A) Calling position of an adult male individual where transparent gular sack is prominent; (B) Ventral aspect of hand with rounded, disked fingertips; (C) Ventral aspect of foot with rounded disked, reddish toe tips.
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.