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Text-fig. 4. Most parsimonious trees obtained after addition of Virginianthus (with "Liliacidites" minutus pollen) to the (A) D&E and (B) J/M trees. Relative parsimony of alternative positions of Virginianthus is indicated as in Text-fig. 2; abbreviations as in Text-fig. 1. in Early Cretaceous Monocots: A Phylogenetic Evaluation
Text-fig. 4. Most parsimonious trees obtained after addition of Virginianthus (with "Liliacidites" minutus pollen) to the (A) D&E and (B) J/M trees. Relative parsimony of alternative positions of Virginianthus is indicated as in Text-fig. 2; abbreviations as in Text-fig. 1.
Text-fig. 2. Representative most parsimonious trees obtained after addition of Liliacidites to (A) the D&E tree (Text-fig. 1) and (B) the J/M tree, with relationships among major clades based on the plastid genome analyses of Jansen et al. (2007) and Moore et al. (2007). Thicker lines indicate all most parsimonious (MP), one step less parsimonious (MP+1), and two step less parsimonious (MP+2) positions for Liliacidites. Abbreviations as in Text-fig. 1. in Early Cretaceous Monocots: A Phylogenetic Evaluation
Text-fig. 2. Representative most parsimonious trees obtained after addition of Liliacidites to (A) the D&E tree (Text-fig. 1) and (B) the J/M tree, with relationships among major clades based on the plastid genome analyses of Jansen et al. (2007) and Moore et al. (2007). Thicker lines indicate all most parsimonious (MP), one step less parsimonious (MP+1), and two step less parsimonious (MP+2) positions for Liliacidites. Abbreviations as in Text-fig. 1.
Text-fig. 3. One of two most parsimonious trees obtained after addition of Anacostia (with Similipollis pollen) to the D&E tree. Relative parsimony of alternative positions of Anacostia is indicated as in Text-fig. 2; abbreviations as in Text-fig. 1. in Early Cretaceous Monocots: A Phylogenetic Evaluation
Text-fig. 3. One of two most parsimonious trees obtained after addition of Anacostia (with Similipollis pollen) to the D&E tree. Relative parsimony of alternative positions of Anacostia is indicated as in Text-fig. 2; abbreviations as in Text-fig. 1.
Text-fig. 1. D&E tree of Endress and Doyle (2009), from the combined morphological and molecular analysis of Doyle and Endress (2000), with modifications based on more recent data, showing the inferred evolution of the reticulum grading character (39). Boxes under names of taxa indicate their character state; shading of branches indicates their reconstructed state based on parsimony optimization with MacClade (Maddison and Maddison 2003). Nymph = Nymphaeales, Aust = Austrobaileyales, Chlor = Chloranthaceae, Piper = Piperales, Ca = Canellales, Magnol = Magnoliales. in Early Cretaceous Monocots: A Phylogenetic Evaluation
Text-fig. 1. D&E tree of Endress and Doyle (2009), from the combined morphological and molecular analysis of Doyle and Endress (2000), with modifications based on more recent data, showing the inferred evolution of the reticulum grading character (39). Boxes under names of taxa indicate their character state; shading of branches indicates their reconstructed state based on parsimony optimization with MacClade (Maddison and Maddison 2003). Nymph = Nymphaeales, Aust = Austrobaileyales, Chlor = Chloranthaceae, Piper = Piperales, Ca = Canellales, Magnol = Magnoliales.
Text-fig. 5. Most parsimonious trees obtained after addition of the Pennipollis plant to the (A) D&E and (B) J/M trees. Relative parsimony of alternative positions of the Pennipollis plant is indicated as in Text-fig. 2; abbreviations as in Text-fig. 1. in Early Cretaceous Monocots: A Phylogenetic Evaluation
Text-fig. 5. Most parsimonious trees obtained after addition of the Pennipollis plant to the (A) D&E and (B) J/M trees. Relative parsimony of alternative positions of the Pennipollis plant is indicated as in Text-fig. 2; abbreviations as in Text-fig. 1.
Figure 2 in Faunistic and zoogeographical composition and preliminary evaluations of some ecological features of the subfamily Staphylininae (Coleoptera: Staphylinidae) of the Central Anatolian Region of Turkey
Figure 2. Number of determined species according to genera, number of species represented in Turkish fauna, and their representation percentages.
Figure 1. DNA extraction with two different protocols from different noninvasive samples. Lines 1, 3, 5 in Evaluation of methods for molecular sex-typing of three heron species from different DNA sources
Figure 1. DNA extraction with two different protocols from different noninvasive samples. Lines 1, 3, 5, and 7: DNA extraction with commercial kit; Lines 2, 4, 6, and 8: DNA extracted with modified standard protocol. Lines 1–2: eggshells (Grey Heron); lines 3–4: eggshell swabs (Grey Heron); lines 5–6: pin feathers (Purple Heron); lines 7–8: contour feathers (Great Egret); 9: negative control; M: molecular marker.
Figure 2. Heron sex-typing with 2550F in Evaluation of methods for molecular sex-typing of three heron species from different DNA sources
Figure 2. Heron sex-typing with 2550F/2718R primers. Lines 1–7: Purple Heron nestlings, males (600 bp for Z chromosome); 8–10: Great Egret nestlings, females (600 bp for Z chromosome and 450 bp for W chromosome); 11: negative control; M: molecular marker.
Figure 3 in Evaluation of water-soluble dyes to mark internal structures of Lepidoptera via larval feeding
Figure 3 Development (days) of S. frugiperda larvae fed an artificial diet containing Ponceau, Methylene Blue, Rhodamine B, Eosin- Nigrosine and Coomassie dyes.(ns indicates that treatments did not differ from each other; bars followed by the same letter within the same dye are not significantly different by Tukey 's test at 0.05 significance).
Figure 2 in Evaluation of water-soluble dyes to mark internal structures of Lepidoptera via larval feeding
Figure 2 Mortality (%) ofS.frugiperda larvae fed an artificial diet containing water-soluble dyes (ns indicates that the treatments did not differ from each other; bars followed by the same letter within the same dye are not significantly different by Tukey 's test at 0.05 significance). Data corrected by Abbott 's formula.
Figure 1 Spermatophores retrieved from S in Evaluation of water-soluble dyes to mark internal structures of Lepidoptera via larval feeding
Figure 1 Spermatophores retrieved from S. frugiperda mated adult females whose larvae were fed with water-soluble dyes. (A) control insect (without dye); (B) Methylene Blue; (C) Coomassie; (D) Ponceau; (E) Rhodamine B; (F) Eosin - Nigrosin.
Figure 1 in Comparative evaluation of taxonomic and functional diversities of leaf-litter ants of the Brazilian Atlantic Forest
Figure 1. Map of the study area in the state of Bahia (A), Brazil (B), showing the locations of the 65 Atlantic Forest sites (C).
Figure 3 in Comparative evaluation of taxonomic and functional diversities of leaf-litter ants of the Brazilian Atlantic Forest
Figure 3. Relationship between number of functional groups (classifications A: FC-A and B: FC-B) with ant richness in 65 localities of the Atlantic Forest biome in Bahia state, Brazil. Appendix 1. List of ant species registered in 26 municipalities and 65 localities of Atlantic Forest in Bahia state, Brazil. Municipalities: A–Z; number in parentheses represents the number of locations sampled by municipality.
Figure 2 in Comparative evaluation of taxonomic and functional diversities of leaf-litter ants of the Brazilian Atlantic Forest
Figure 2. Species accumulation curves based on the number of ant species (observed richness) sampled in different localities of the Brazilian Atlantic Forest. Filled circle = all data; filled diamond = all data except singletons and doubletons; unfilled circle = singletons and doubletons only.
Figure 4 in Evaluation of nickel-induced brain injuries in rats via oxidative stress and apoptosis: attenuating effects of hyperoside
Figure 4. Morphology and location of PAS granules of brain tissues of control (A), Hyp-treated (B), Ni-treated (C), and Ni + Hyp-treated (D) rats. Homogeneous PAS staining was observed in the control group (A) and the Hyp-treated (B) groups. Clusters of granules shown inside square (C) and by black arrow (D), respectively (200× magnification).
Figure 3 in Evaluation of nickel-induced brain injuries in rats via oxidative stress and apoptosis: attenuating effects of hyperoside
Figure 3. Histological views of brain tissues of control (A), Hyp-treated (B), Ni-treated (C), and Ni + Hyp-treated (D) rats. Small blood vessels (BV) from pia mater penetrate the cerebral cortex substance pyramidal cells (PC) with apical dendrites closely associated with smaller, round glial cells (GC) (A and B). Perivascular inflammation around a blood vessel (inside square) (C) and perivascular inflammatory cell infiltrates in hematoxylin and eosin-stained brain tissue (D) (200× magnification).
Figure 5 in Evaluation of nickel-induced brain injuries in rats via oxidative stress and apoptosis: attenuating effects of hyperoside
Figure 5. Brain tissues of control (A) and Hyp (B) groups were negative for Congo red. Amyloid deposits in brain parenchyma and around blood vessels shown inside square (C) and marked by black arrows (D) (200× magnification). Differences in measured parameters among the groups were analyzed with a nonparametric test (Kruskal–Wallis). Dual comparisons between groups exhibiting significant values were evaluated with a Mann–Whitney U test (P <0.05).
Figure 1 in Evaluation of nickel-induced brain injuries in rats via oxidative stress and apoptosis: attenuating effects of hyperoside
Figure 1. Effect of Ni administration on body weight gain. Data are presented as mean ± standard error of mean (SEM) (n = 7). a Significant differences between other studied groups and control (a4 P <0.0001). b Significant differences between other groups studied and Hyp group (b1 P <0.05, b4 P <0.0001). c Significant differences between other groups studied and Ni + Hyp group (c3 P <0.001) by Tukey's multiple range tests.
Figure 1 in Evaluation of the feeding patterns of important mosquito vector species using molecular techniques
Figure 1. Sampling localities of Anopheles sacharovi, Culex pipiens, Culex tritaeniorhynchus populations (1. Kadirli, 2. Düziçi, 3. Türkoğlu, 4. Dörtyol, 5. Kırıkhan, 6. Kozan, 7. Yumurtalık, 8. Karataş, 9. Ceyhan, 10. Tuzla, 11. Tarsus, 12.Huzurkent, 13. Manavgat, 14. Isparta, 15. Burdur, 16. Sandıklı, 17. Akköy, 18. Dalaman, 19. Söke, 20. Manisa).
Figure 2 in Evaluation of the feeding patterns of important mosquito vector species using molecular techniques
Figure 2. Agarose-gel image of cytb gene region of possible hosts (M: marker (100- 1000 bp) 1. Goat; 2. Bird; 3. Human; 4. Cow; 5. Dog; 6. Horse)
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.