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Fig. 6. Short s in Types and functions of mole cricket (Orthoptera: Gryllotalpidae) antennal and palpal sensilla
Fig. 6. Short s. basioconica (×22k and 15k) (sb) (A), arranged in transverse row on the apical part of antennal segment of N. hexadactyla (×900) (B).
Fig. 4 in Types and functions of mole cricket (Orthoptera: Gryllotalpidae) antennal and palpal sensilla
Fig. 4. Transmission electron micrographs of s. chaetica type I and II (A, B) which are not innervated and are dense inside with thick sensillum wall (sw), type III s. chaetica have less dense sensillar lumen (sl) and are innervated with 4 dendrites (d) (C, D).
Fig. 9 in Types and functions of mole cricket (Orthoptera: Gryllotalpidae) antennal and palpal sensilla
Fig. 9. Mole cricket labial and maxillary palps are densely covered with sensilla (× 300) (A). The dominant type is s. chaetica (× 8k) (B), other types include s. coeloconica (×15k) (C) with tip-pore (× 40k) (D), single-wall tip-pore sensilla (× 9k) (E) and club-like s. basioconica (× 11k) (F).
Fig. 1 in Long-term efficacy of two cricket and two liver diets for rearing laboratory fire ant colonies (Hymenoptera: Formicidae: Solenopsis invicta)
Fig. 1. Results of a 1 yr diet study using sugar water and either raw beef liver, raw chicken liver, or crickets to rear colonies of the imported fire ant Solenopsis invicta. A) Mean brood production rating of test colonies with brood: 4 = excel- lent, substantially more brood than workers; 3 = good, brood about equal to workers; 2 = poor, brood substantially less than workers; 1 = bad, only a little brood visible; and 0 = no brood. Colonies were fractionally rated if they ap- peared intermediate. Early in the study, about the end of Mar, we switched from domestic crickets (black squares) to banded crickets (crossed squares) and then back to domestic crickets (black squares) for 6 ant colonies on 6 Jun and then the remaining 7 colonies on 1 Jul. Colonies were eliminated from rating means when the queen died or brood production ceased. B) Percentage of test colonies containing brood plotted against time in months for colonies receiving either beef liver (N =10), chicken liver (N = 10), or crickets (N = 13).
Fig. 4 in Phylogeography and Genetic Structure of the Bush Cricket (Orthoptera, Tettigoniidae) in Southern China.
Fig. 4. Structure clustering results. (A) the posterior probability of each K; (B) the distribution of Delta K values; (C) Bayesian clustering results at K = 9; S1–3 was the groups defined by SOMOVA.
Fig. 3. The genetic distances among populations. A in Phylogeography and Genetic Structure of the Bush Cricket (Orthoptera, Tettigoniidae) in Southern China.
Fig. 3. The genetic distances among populations. A: based on Kimura's 2-parameter; B: based on Tamura 3-parameter.
Fig. 2 in Phylogeography and Genetic Structure of the Bush Cricket (Orthoptera, Tettigoniidae) in Southern China.
Fig. 2. Potential distribution areas of D. fissa in different periods. Potential areas for (A) Current day; (B), Last Glacial Maximum; (C), MidHolocene; (D), year 2070 (RCP 4.5).
Fig. 9 in Phylogeography and Genetic Structure of the Bush Cricket (Orthoptera, Tettigoniidae) in Southern China.
Fig. 9. The dispersed path of D. fissa. A: Central China; B: South China; C: Yunnan-Guizhou Plateau; D: Southeast coastal area; E: Sichuan Basin.
Fig. 7 in Phylogeography and Genetic Structure of the Bush Cricket (Orthoptera, Tettigoniidae) in Southern China.
Fig. 7. Mismatch distributions (left) and Bayesian skyline plots (right) for lineages I, IV, and V of D. fissa based on mitochondrial data.
Fig. 6 in Phylogeography and Genetic Structure of the Bush Cricket (Orthoptera, Tettigoniidae) in Southern China.
Fig. 6. The mitochondrial haplotype network of concatenated sequences. The dotted box represents the five lineages based on divergence time analysis.
Linked collectors and determiners for: New taxa and notes on crickets of the subfamily Landrevinae (Orthoptera: Gryllidae) from Brunei Darussalam, Borneo.
Natural history specimen data linked to collectors and determiners held within, "New taxa and notes on crickets of the subfamily Landrevinae (Orthoptera: Gryllidae) from Brunei Darussalam, Borneo". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="http://bionomia.net/dataset/8718a968-18bd-49fa-aaa9-d8b56f49baa7">https://bionomia.net/dataset/8718a968-18bd-49fa-aaa9-d8b56f49baa7</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/8718a968-18bd-49fa-aaa9-d8b56f49baa7">https://gbif.org/dataset/8718a968-18bd-49fa-aaa9-d8b56f49baa7</a>. Formatted as a Frictionless Data package.
Figure 4 in Mandibular morphology and dietary preferences in two pygmy mole crickets of the genus Xya (Orthoptera: Tridactylidae)
Figure 4. The proportion of detritus in the diet of females (F) and males (M) in (a) Xya pfaendleri and (b) X. variegata as determined based on the postmortem gut content analyses. The box plots show the median (50th percentile) and 25th and 75th quartiles; error bars show the 10th and 90th percentiles. Open circles indicate outliers.
Figure 3 in Mandibular morphology and dietary preferences in two pygmy mole crickets of the genus Xya (Orthoptera: Tridactylidae)
Figure 3. Differences in the surfaces of the (a) left and the (b) right mandibles in Xya pfaendleri and X. variegata. The box plots show the median (50th percentile) and 25th and 75th quartiles; error bars show the 10th and 90th percentiles.
Figure 1 in Mandibular morphology and dietary preferences in two pygmy mole crickets of the genus Xya (Orthoptera: Tridactylidae)
Figure 1. Dorsal and ventral views of the left and right mandibles of Xya pfaendleri and X. variegata. The microstructures of the mandibles were documented by scanning electron microscopy (SEM; JEOL JSM-6610LV): SEI, 12 kV, WD 50 mm, SS30, 65× magnification.
Figure 2 in Mandibular morphology and dietary preferences in two pygmy mole crickets of the genus Xya (Orthoptera: Tridactylidae)
Figure 2. Comparison of the measured parameters of the mandibles in females (gray boxes) and males (white boxes) of Xya pfaendleri and X. variegata (Tridactylidae). a, d: length of the mandible (distance between the mandibular junction and the peak of the first incisor); b, e: surface of the molar ridge; c, f: number of molar slats. The box plots show the median (50th percentile) and 25th and 75th quartiles; error bars show the 10th and 90th percentiles. Filled symbols indicate outliers.
Figure 5 in Mandibular morphology and dietary preferences in two pygmy mole crickets of the genus Xya (Orthoptera: Tridactylidae)
Figure 5. The food niche breadths in males (M) and females (F) of (a) Xya pfaendleri and (b) X. variegata (Orthoptera: Tridactylidae). The food niche breadth was cumulatively evaluated based on the Gini-Simpson index. The box plots show the median (50th percentile) and the 25th and 75th quartiles; error bars show the 10th and 90th percentiles.
Figure 8 in First results of a faunistic survey on the Orthoptera of Jadovnik Mountain, southwestern Serbia, with data on the calling songs of some bush cricket species
Figure 8. SEM image of the stridulatory file in Poecilimon affinis dinaricus, Ogoreljača–Mali Jadovnik (meadow).
Figure 10 in First results of a faunistic survey on the Orthoptera of Jadovnik Mountain, southwestern Serbia, with data on the calling songs of some bush cricket species
Figure 10. Poecilimon pseudornatus, oscillograms of male calling song at 28 °C from: A) Sopotnica Ra; B) Ogoreljača–Mali Jadovnik (roadside).
Figure 7 in First results of a faunistic survey on the Orthoptera of Jadovnik Mountain, southwestern Serbia, with data on the calling songs of some bush cricket species
Figure 7. Calling song of Poecilimon affinis dinaricus males from Ogoreljača–Mali Jadovnik (meadow). Syllables at different temperatures: A) syllable at 20 °C; B) syllable at 28 °C.
Figure 3 in First results of a faunistic survey on the Orthoptera of Jadovnik Mountain, southwestern Serbia, with data on the calling songs of some bush cricket species
Figure 3. Isophya clara, oscillograms of male calling song from Ovčar-Kablar Gorge. A) 6 syllables; B) syllable with after-click.
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.