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Comparative mitochondrial genome and phylogenetic analysis of malaria mosquitoes Anopheles hyrcanus and Anopheles messeae supplementary files
<p><strong>T</strong><strong><span>able</span></strong><strong> S1.</strong> This study encompassed 105 species, along with their corresponding taxonomy and GenBank registration numbers.</p> <p><strong>Figure S1</strong> Inferred secondary structures of tRNAs in the mt genome of <em>An. </em><em><span>h</span></em><em>yrcanus</em><em> </em><span>(A)</span><em> </em><span>and </span><em>An. </em><em><span>m</span></em><em>esseae</em><em> </em><span>(B)</span>, with corresponding amino acids labeled next to the tRNAs.</p>
Figs 79–92 in Comparative analysis of male calling signals in closely related species of Macropsis Lewis, 1836 (Homoptera: Auchenorrhyncha: Cicadellidae: Eurymelinae: Macropsini) reveals possible ways of evolution of the signal temporal pattern
Figs 79–92. Oscillograms of male calling signals: 79–82 — Evacanthus asiaticus; 83–88 — Limotettix (Scleroracus) russeolus; 89–92 — Hephathus nanus. Faster oscillograms of the parts of signals indicated as "86–88" and "91–92" are given under the same numbers. Рис. 79–92. Осциллограммы приЗывных сигналов: 79–82 — Evacanthus asiaticus; 83–88 — Limotettix (Scleroracus) russeolus; 89– 92 — Hephathus nanus. Фрагменты сигналов, обоЗначенные цифрами "86–88" и "91–92", представлены на осциллограммах под такими же номерами.
Figs 64–78 in Comparative analysis of male calling signals in closely related species of Macropsis Lewis, 1836 (Homoptera: Auchenorrhyncha: Cicadellidae: Eurymelinae: Macropsini) reveals possible ways of evolution of the signal temporal pattern
Figs 64–78. Oscillograms of male calling signals: 64–65 — Handianus fartilis; 66–69 — Aconurella diplachnis; 70–78 — Fangamanus tripunctatus. Faster oscillograms of the parts of signals indicated as "67–69" and "74–78" are given under the same numbers. Рис. 64–78. Осциллограммы приЗывных сигналов: 64–65 — Handianus fartilis; 66–69 — Aconurella diplachnis; 70–78 — Fangamanus tripunctatus. Фрагменты сигналов, обоЗначенные цифрами "67–69" и "74–78", представлены на осциллограммах под такими же номерами.
Figs 54–63 in Comparative analysis of male calling signals in closely related species of Macropsis Lewis, 1836 (Homoptera: Auchenorrhyncha: Cicadellidae: Eurymelinae: Macropsini) reveals possible ways of evolution of the signal temporal pattern
Figs 54–63. Oscillograms of male calling signals: 54–57 — Macropsis megerlei; 58–63 — M. ornata. Faster oscillograms of the parts of signals indicated as "56–57" and "61–63" are given under the same numbers. Рис. 54–63. Осциллограммы приЗывных сигналов: 54–57 — Macropsis megerlei; 58–63 — M. ornata. Фрагменты сигналов, обоЗначенные цифрами "56–57" и "61–63", представлены на осциллограммах под такими же номерами.
Figs 39–53 in Comparative analysis of male calling signals in closely related species of Macropsis Lewis, 1836 (Homoptera: Auchenorrhyncha: Cicadellidae: Eurymelinae: Macropsini) reveals possible ways of evolution of the signal temporal pattern
Figs 39–53. Oscillograms of male calling signals: 39–47 — Macropsis milkoi; 48–53 — M. aselae. Faster oscillograms of the parts of signals indicated as "40", "46–47", and "52–53" are given under the same numbers. Рис. 39–53. Осциллограммы приЗывных сигналов: 39–47 — Macropsis milkoi; 48–53 — M. aselae. Фрагменты сигналов, обоЗначенные цифрами "40", "46–47" и "52–53", представлены на осциллограммах под такими же номерами.
Fig. 2 in Gut-content analysis in four species, combined with comparative analysis of trophic traits, suggests an araneophagous habit for the entire family Palpimanidae (Araneae)
Fig. 2 Comparison of relative 1 conspeccfics spcders cnsects 1 frequency of conspecifics (can- A B nibalism), heterospecific spiders 0.9 0.9 (araneophagy), and insects in 0.8 0.8 the gut of P . gibbulus A, P . 0.7 0.7 potteri B , Diaphorocellus C and frequency Otiothops D . Proportions are 0.6 0.6 estimated per all individuals in e 0.5 0.5 a class (male, female, juvenile). 0.4 0.4 Frequency of cannibalism can be overestimated (see "Discus- Rela 0.3 0.3 sion" for more details), thus 0.2 0.2 should be interpreted with 0.1 0.1 caution 0 0 male female female juvencle adult juvencle adult
Fig. 3 in Gut-content analysis in four species, combined with comparative analysis of trophic traits, suggests an araneophagous habit for the entire family Palpimanidae (Araneae)
Fig. 3 Phylogeny of Palpimanidae plus three other families on the genus level, with estimates of the probabilities of each of five traits at nodes. The fuller the symbol, the higher the probability of a presence of the trait. For trait values at terminals see Table S7
Fig. 5 in Comparative Analysis of the Ecological Functions of Dung Removal and Seed Dispersal among Two Telecoprid and Two Paracoprid Dung Beetles (Coleoptera: Scarabaeidae: Scarabaeinae)
Fig. 5. Box plots of the median, first, and third quartile, and lower and upper limits of dung removal by standardized 1-g biomass of Canthon rutilans cyanescens, Deltochilum multicolor, Dichotomius sericeus, and Phanaeus splendidulus exposed to dog feces for two and seven days. Plots with the same letter are not significantly different (Tukey test, P> 0.05).
Fig. 4 in Comparative Analysis of the Ecological Functions of Dung Removal and Seed Dispersal among Two Telecoprid and Two Paracoprid Dung Beetles (Coleoptera: Scarabaeidae: Scarabaeinae)
Fig. 4. Comparative analysis of dung removal and secondary dispersal of small and large seeds by single male/ female pair of Canthon rutilans cyanescens (Cr), Deltochilum multicolor (Dm), Dichotomius sericeus (Ds), and Phanaeus splendidulus (Ps) exposed to dog feces for two and seven days. Squares with the same letter and color are not significantly different (Tukey test, P> 0.05).
Fig. 3 in Comparative Analysis of the Ecological Functions of Dung Removal and Seed Dispersal among Two Telecoprid and Two Paracoprid Dung Beetles (Coleoptera: Scarabaeidae: Scarabaeinae)
Fig. 3. Box plots of the median, first, and third quartile, and lower and upper limits of dung removal and secondary seed dispersal by two paracoprid dung beetles as single male/female pair and three male/female pairs exposed to dog feces for two, seven, and 21 days. A) Dung removal capacity, B) Small seed dispersal, and C) Large seed dispersal by Dichotomius sericeus. D) Dung removal capacity, E) Small seed dispersal, and F) Large seed dispersal by Phanaeus splendidulus. Plots with the same letter are not significantly different (Tukey test, P> 0.05).
Fig. 1 in Comparative Analysis of the Ecological Functions of Dung Removal and Seed Dispersal among Two Telecoprid and Two Paracoprid Dung Beetles (Coleoptera: Scarabaeidae: Scarabaeinae)
Fig. 1. Arenas for the study of dung removal and secondary seed dispersal by dung beetles. A) Arena for telecoprids with 30 g of dyed feces divided into three portions of 10 g each with a variable number of artificial seeds, B) Closed arena covered with veil-type fabric, C) Arena protected from rain. D, E, and F show the same sequence for the arenas for paracoprids.
Fig. 2 in Comparative Analysis of the Ecological Functions of Dung Removal and Seed Dispersal among Two Telecoprid and Two Paracoprid Dung Beetles (Coleoptera: Scarabaeidae: Scarabaeinae)
Fig. 2. Box plots of the median, first, and third quartile, and lower and upper limits of dung removal and secondary seed dispersal by two telecoprid dung beetles as single male/female pair and three male/female pairs exposed to dog feces for two, seven, and 21 days. A) Dung removal capacity, B) Small seed dispersal, and C) Large seed dispersal by Canthon rutilans cyanescens. D) Dung removal capacity, E) Small seed dispersal, and F) Large seed dispersal by Deltochilum multicolor. Plots with the same letter are not significantly different (Tukey test, P> 0.05).
Fig. 4 in Comparative analysis of peripheral blood reveals transcriptomic adaptations to extreme environments on the Qinghai-Tibetan Plateau in the gray wolf (Canis lupus chanco)
Fig. 4 Reconstructed mitochondrial DNA tree of the worldwide distributed wolves. The numbers at each node are the Bayesian posterior probabilities (right) and ML bootstrap propor- tions (left)
Fig. 3 in Comparative analysis of peripheral blood reveals transcriptomic adaptations to extreme environments on the Qinghai-Tibetan Plateau in the gray wolf (Canis lupus chanco)
Fig. 3 Scatterplot of enriched KEGG pathways for DEGs between the Tibetan and lowland wolves. The enrichment factor is the ratio of the DEG number to the total gene number in the pathway. The dot size and color represent the gene number and the range of the p value respectively
Fig. 1 in Comparative analysis of peripheral blood reveals transcriptomic adaptations to extreme environments on the Qinghai-Tibetan Plateau in the gray wolf (Canis lupus chanco)
Fig. 1 Gene expression profiles of blood in Tibetan and lowland wolves. a Boxplot of the log transformed FPKM expression values across eight wolf blood samples. FPKM: fragments per kilobase of exon per million fragments. The solid horizontal line represents the median, and the box
FIGURE 6 in Comparative analysis of rDNA distribution in 29 species of Begonia sect. Coelocentrum Irmsch.
FIGURE 6. Simultaneous localization of 5S (red) and 45S (green) rDNA sites in B. guangxiensis (a) and B. longgangensis (b). Bars, 5μm
FIGURE 3 in Comparative analysis of rDNA distribution in 29 species of Begonia sect. Coelocentrum Irmsch.
FIGURE 3. Simultaneous localization of 5S (red) and 45S (green) rDNA sites in B. zhuoyunii ined. (a), B. pengii (b), B. biflora (c), B. cavaleriei (d), B. morsei (e), B. bamaensis (f), and B. pseudoleprosa (g). Bars, 5μm
FIGURE 2 in Comparative analysis of rDNA distribution in 29 species of Begonia sect. Coelocentrum Irmsch.
FIGURE 2. Simultaneous localization of 5S (red) and 45S (green) rDNA sites in B. austroguangxiensis (a), B. linguiensis (b), B. suboblata (c), B. daxinensis (d), B. retinervia (e), and B. subcoriacea (f). Bars, 5μm
FIGURE 1 in Comparative analysis of rDNA distribution in 29 species of Begonia sect. Coelocentrum Irmsch.
FIGURE 1. Somatic chromosomes at metaphase of B. biflora (a), B. cavaleriei (b), B. huangii (c), B. longistyla (d), B. luochengensis (e), B. masoniana (f), B. morsei (g), B. pseudodaxinensis (h), B. suboblata (i), and B. longgangensis (j). The DAPI-stained chromosomes were converted into a black-white image to clearly show centromere position. The arrows from the above pictures indicate longer metacentric chromosomes. Bars, 5μm
FIGURE 5 in Comparative analysis of rDNA distribution in 29 species of Begonia sect. Coelocentrum Irmsch.
FIGURE 5. Simultaneous localization of 5S (red) and 45S (green) rDNA sites in B. jingxiensis (a), B. huangii (b), B. pseudodaxinensis (c), B. chongzuoensis (d), B. luzhaiensis (e), B. sp. nov. (f), and B. luochengensis (g). Bars, 5μm
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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.