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4,287 results for “Asteraceae”
FIGURES 63–69 in American Asteraceae-feeding Astrotischeria species with a highly modified, three-lobed valva in the male genitalia (Lepidoptera, Tischeriidae)
FIGURES 63–69. LEAF MINES OF Astrotischeria trilobata DIŠKUS & STONIS, sp. nov., VILCAbAMbA, ECUADOR.
FIGURE 2 in American Asteraceae-feeding Astrotischeria species with a highly modified, three-lobed valva in the male genitalia (Lepidoptera, Tischeriidae)
FIGURE 2. MORPHOLOGy OF FEMALE GENITALIA OF Astrotischeria karsholti PUPLESIS & DIŠKUS, THE TyPE SPECIES OF Astrotischeria. NOTE: THE FIGURED OVIPOSITOR bELONGS TO A NON-Astrotischeria SPECIES, Coptotriche angusticolella (DUPONCHEL) (AFTER PUPLESIS & DIŠKUS 2003).
Suppl. material 2 from: Heng L-M, Zheng Y-L, Zhao Y-B, Wang Y-J (2018) Radiation of members of the Soroseris hookeriana complex (Asteraceae) on the Qinghai-Tibetan Plateau and their proposed taxonomic treatment. PhytoKeys 114: 11-25. https://doi.org/10.3897/phytokeys.114.29914
The 50% majority rule consensus tree derived from Bayesian inference of the combined sequences of nuclear internal transcribed spacer, psbA-trnH and matK : Explanation note: Posterior probabilities and bootstrap percentages are indicated above and below the branches, respectively. The samples named according to FOC (2011) or NCBI, Stebbins (1940) and the present study are listed from left to right.
Suppl. material 1 from: Heng L-M, Zheng Y-L, Zhao Y-B, Wang Y-J (2018) Radiation of members of the Soroseris hookeriana complex (Asteraceae) on the Qinghai-Tibetan Plateau and their proposed taxonomic treatment. PhytoKeys 114: 11-25. https://doi.org/10.3897/phytokeys.114.29914
The main morphological difference amongst members of the Soroserishookeriana complex and the closely related species :
FIGURE 3 in Aphis (Hemiptera, Aphididae) species living on Baccharis (Asteraceae) in southern South America, with description of three new species
FIGURE 3. Aphis fuentesi Nieto Nafría & Ortego, sp. n. A–D apterous viviparous females; A, specimen moderately sclerotized; B, specimen extensively sclerotized; C, dorso-abdominal reticulation; D, siphunculus and marginal tubercles on abdominal segments 6 and 7. F–G, alate viviparous females; F, habitus; G, antennal segment III. H, oviparous female. I, male. The scales vary according to specimens or parts photographed; see measurements in Table 2.
FIGURE 1 in Aphis (Hemiptera, Aphididae) species living on Baccharis (Asteraceae) in southern South America, with description of three new species
FIGURE 1. Aphis ingeborgae Nieto Nafría & Brown, sp. n. A–G, apterous viviparous females; A, specimen extensively sclerotized; B, specimen moderately sclerotized; C, dorso-cephalic reticulation; D, dorso-abdominal reticulation; E, prothoracic marginal tubercle; F, three different marginal tubercles on abdominal segment 1; G, marginal tubercle on an intermediate abdominal segment. H–I, alate viviparous female; H, habitus; I, antennal segment III. The scales vary according to specimens or parts photographed; see measurements in Table 1.
FIGURE 2 in Aphis (Hemiptera, Aphididae) species living on Baccharis (Asteraceae) in southern South America, with description of three new species
FIGURE 2. Aphis conspicua Nieto Nafría & Mier Durante, sp. n. A–D, apterous viviparous female; A, specimen with intermediate dorsal sclerotisation; B, dorso-thoracic reticulation; C, marginal tubercles on metathorax (small one placed partially on the pigmented sclerite) and abdominal segments 1, 2 and 3; D, dorso-abdominal reticulation. E–F, Alate viviparous females; E, head plus a part of prothorax, and a part of metathorax plus abdomen; F, antennal segment III. The scales vary according to specimens or parts photographed; see measurements in Table 1.
Fig. 6 in How many taxa? Spatiotemporal evolution and taxonomy of Amphoricarpos (Asteraceae, Carduoideae) on the Balkan Peninsula
Fig. 6 Morphological variation in Amphoricarpos on the Balkan Peninsula based on 17 metric characters and six ratios. a, c Principal component analysis. b, d Canonical discriminant analyses. Labelling and grouping in a and b follow Blečić and Mayer (1967), in c and d they reflect the five BAPS clusters shown in Fig. 5b–e
Fig. 2 in How many taxa? Spatiotemporal evolution and taxonomy of Amphoricarpos (Asteraceae, Carduoideae) on the Balkan Peninsula
Fig. 2 Relationships of Amphoricarpos from the Balkan Peninsula inferred from phylogenetic analyses of Internal Transcribed Spacer (ITS) sequences. a Bayesian consensus phylogram; numbers above branches are bootstrap values>50 %, those below branches PP values>0.50. b Bayesian consensus chronogram (obtained
Fig. 1 in How many taxa? Spatiotemporal evolution and taxonomy of Amphoricarpos (Asteraceae, Carduoideae) on the Balkan Peninsula
Fig. 1 Sampled populations of Amphoricarpos on the Balkan Peninsula. The inserts show the position of the sampled area in southeastern Europe and a plant from population 26. The taxonomic assignment follows Blečić and Mayer (1967)
Fig. 4 in How many taxa? Spatiotemporal evolution and taxonomy of Amphoricarpos (Asteraceae, Carduoideae) on the Balkan Peninsula
Fig. 4 NeighborNet diagram based on uncorrected P distances derived from AFLP data of Amphoricarpos from the Balkan Peninsula. Numbers positioned along the splits are bootstrap values derived from Neighbourjoining analysis (1,000 replicates). Populations are coded as in Fig. 1 and
Fig. 3 in How many taxa? Spatiotemporal evolution and taxonomy of Amphoricarpos (Asteraceae, Carduoideae) on the Balkan Peninsula
Fig. 3 Relationships of Amphoricarpos from the Balkan Peninsula inferred from phylogenetic analyses of plastid rps16–trnK sequences. a, Bayesian consensus phylogram; numbers above branches are bootstrap values>50 %, those below branches PP values>0.50. b, Statistical parsimony network. Small black dots represent unsampled haplotypes, numbers are population identifiers as in Fig. 1 and Table 1
Fig. 2 in Divergence time estimation in Cichorieae (Asteraceae) using a fossil-calibrated relaxed molecular clock
Fig. 2 Chronogram of Cichorieae produced by the program BEAST based on ITS1 and ITS2 sequences (unconstrained topology; maximum clade credibility tree with mean node heights obtained by stem group node calibration). Posterior probabilities of nodes are shown
Fig. 5 in Molecular and phytochemical systematics of the subtribe Hypochaeridinae (Asteraceae, Cichorieae)
Fig. 5 Overview of the distribution of hypocretenolides within the phylogenetic context of the Hypochaeridinae
Fig. 3 in Molecular and phytochemical systematics of the subtribe Hypochaeridinae (Asteraceae, Cichorieae)
Fig. 3 Overview of the distribution of caffeoyl tartaric acid derivatives within the phylogenetic context of the Hypochaeridinae
Fig. 2 in Flowering phenology of co-occurring Asteraceae: a matter of climate, ecological interactions, plant attributes or of evolutionary relationships among species?
Fig. 2 Number of Asteraceae species growing in Chaco Serrano forests of La Serranita-Los Aromos that bear flowers during each month of the year; for calculation, see text in Material and methods Section
Fig. 1 in Flowering phenology of co-occurring Asteraceae: a matter of climate, ecological interactions, plant attributes or of evolutionary relationships among species?
Fig. 1 Diagram of phylogenetic relationships between Asteraceae taxa studied in this work (adapted from Panero and Crozier 2008; Panero and Funk 2008)
Fig. 4 in Flowering phenology of co-occurring Asteraceae: a matter of climate, ecological interactions, plant attributes or of evolutionary relationships among species?
Fig. 4 Plot of PCA scores for 43 co-occurring Asteraceae species in Chaco Serrano forests of La Serranita-Los Aromos, showing first two principal component axes from analysis of flowering phenology considering plant traits and taxonomic membership. Vectors corre-
FIGURE 4 in Staurochlamys (Neurolaeneae, Asteraceae): an endemic genus from Cerrado, Brazil
FIGURE 4. Species distribution models map of Staurochlamys burchellii (Neurolaeneae, Asteraceae) under three climate scenarios: Interglacial Maximum (A), Glacial Maximum (B), and current (C).
FIGURE 5 in Staurochlamys (Neurolaeneae, Asteraceae): an endemic genus from Cerrado, Brazil
FIGURE 5. Stable areas map of Staurochlamys burchellii (Neurolaeneae, Asteraceae) considering the Interglacial Maximum, Glacial Maximum and current climate scenarios. Brazilian states: BA—Bahia, CE—Ceará, GO—Goiás, MG—Minas Gerais, MA—Maranhão, MS—Mato Grosso do Sul, MT—Mato Grosso, PA—Pará, PI—Piauí, PE—Pernambuco, and DF—Distrito Federal. Ocean: AO—Atlantic Ocean.
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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.
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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.