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FIGURE 2. Lessingianthus semirii. A. Habit. B. Head. C. Capitulescence. Lessingianthus monocephalus. D. Habit. E. Head. F. Capitulescence. A–C in Contribution to the Vernonieae (Asteraceae) of the Cerrado: a transfer to Lessingianthus, in a new rank and with a new name
FIGURE 2. Lessingianthus semirii. A. Habit. B. Head. C. Capitulescence. Lessingianthus monocephalus. D. Habit. E. Head. F. Capitulescence. A–C by G. Antar; D–F by C. Siniscalchi.
FIGURE 6. Leaf base and stem indument. A. Lessingianthus semirii. B. Lessingianthus monocephalus. A in Contribution to the Vernonieae (Asteraceae) of the Cerrado: a transfer to Lessingianthus, in a new rank and with a new name
FIGURE 6. Leaf base and stem indument. A. Lessingianthus semirii. B. Lessingianthus monocephalus. A by G.M. Antar; B by C. Siniscalchi.
FIGURE 5 in Contribution to the Vernonieae (Asteraceae) of the Cerrado: a transfer to Lessingianthus, in a new rank and with a new name
FIGURE 5. Holotype of Lessingianthus monocephalus (Gardner) Robinson (BM-000799067). Image by courtesy of Natural History Museum, London; reproduced with permission.
FIGURE 3 in Contribution to the Vernonieae (Asteraceae) of the Cerrado: a transfer to Lessingianthus, in a new rank and with a new name
FIGURE 3. Isotype of Lessingianthus semirii Antar & Loeuille (NY-00274886). Image by courtesy of New York Botanical Garden, New York; reproduced with permission.
FIGURE 3. 50 in The phylogenetic position of Coniarthonia and the transfer of Cryptothecia miniata to Myriostigma (Arthoniaceae, lichenized ascomycetes)
FIGURE 3. 50% majority-rule consensus tree inferred from mtSSU sequence data produced by a Bayesian analysis and showing the phylogenetic relationships among 45 specimens of Arthoniales. PP values are shown at internal branches.
FIGURE 1 in The phylogenetic position of Coniarthonia and the transfer of Cryptothecia miniata to Myriostigma (Arthoniaceae, lichenized ascomycetes)
FIGURE 1. Coniarthonia megaspora, isotype (ABL). A. habitus. B. ascospores. C. asci. D. section through apothecium. Scale: A = 0.5 cm, B = 10 μm, C = 20 μm, D = 50 μm.
FIGURE 2 in The phylogenetic position of Coniarthonia and the transfer of Cryptothecia miniata to Myriostigma (Arthoniaceae, lichenized ascomycetes)
FIGURE 2. Myriostigma miniatum, isoepitype (ABL). A. habitus. B. detail showing ascomata. C. ascospore in median optical section showing large lumina in the center and small lumina in the periphery. D. the same ascospore in optical surface view showing only small lumina. Scale: A = 0.5 cm, B = 0.5 mm, C–D = 10 μm.
FIGURE 1 in A new Disporopsis (Asparagaceae) transferred from Polygonatum
FIGURE 1. Somatic chromosome count of Disporopsis bodinieri from root tips of plants cultivated by the author, 2n = 2x = 40, Floden et al. 1924 (TENN), protocol following Floden (2014).
FIGURE 1 in Towards a phylogenetic classification of species belonging to the diatom genus Cyclotella (Bacillariophyceae): Transfer of species formerly placed in Puncticulata, Handmannia, Pliocaenicus and Cyclotella to the genus Lindavia
FIGURE 1. Diagramatic representation of the arrangement of key morphological features in Cyclotella and related genera. Cyclotella sensu stricto (upper right) have a rimoportula within the ring of marginal fultoportulae and located on a costa. In Discostella (upper left), the rimoportula is also located within the ring of marginal fultoportulae, and both types of processes are located between costae. In Tertiarius (lower right), the internal opening of the rimoportula is positioned laterally on a fultoportula-bearing costa (typically, see text). Lindavia (lower left) has the synapomorphic condition that both the internal and external openings of the rimoportula are on the valve face. VM = valve mantle, C = costae, LP = rimoportula (labiate process), SP = fultoportula (strutted process).
FIGURE 3 in Molecular and morphological data support the transfer of the monotypic Iranian genus Alococarpum to Prangos (Apiaceae)
FIGURE 3 Bayesian phylogenetic tree of nrITS/ETS nucleotide sequences. Posterior probabilities values and bootstrap values of MP are shown.
FIGURE 1 in Molecular and morphological data support the transfer of the monotypic Iranian genus Alococarpum to Prangos (Apiaceae)
FIGURE 1 Surface of mericarps (A, B) and general view of mericarps (C–F), scale interval (C–F) = 5 mm: A. Alococarpum erianthum (Iran, Azerbaijan, Szovitz 565 (P02422277); B. Prangos cheilanthifolia (Iran, Esfahan prov., 31 May 1974, Iranshahr s.n. (TARI); C. Alococarpum erianthum (see Fig. 1a); D. P. cheilanthifolia (see Fig. 1b); E. P. tschimganica (Uzbekistan, Tashkent prov., 17 Aug. 1958, Pavlov 19 (MW); F. P. ledebourii (Kazakhstan, Jungar Alatau, 01 Jul. 1974, Pimenov 501 (MW).
FIGURE 2 in Molecular and morphological data support the transfer of the monotypic Iranian genus Alococarpum to Prangos (Apiaceae)
FIGURE 2 Mericarps cross sections, scale interval = 1 mm: A. Cachrys libanotis picture by Pimenov & Tikhomirov (1983); B. Bilacunaria microcarpa picture by Pimenov & Tikhomirov (1983); C. Alococarpum erianthum (Iran, Azerbaijan, Szovitz 565 (P02422277); D. Prangos ferulacea (Turkey, Konya, 15 Aug. 2008, Pimenov & Kljuykov 79 (MW): 1—rib, 2—"epimesocarp", 3—inner mesocarp, 4—vascular bundles, 5—secretory ducts, 6—endosperm. All designations of the Alococarpum erianthum and following figures are the same; E. P. ledebourii (Kazakhstan, Jungar Alatau, 01 Jul. 1974, Pimenov 501 (MW); F. P. peucedanifolia (Armenia turcica, Kharput, 28 May 1889, Stapf 554 (LE); G. P. tschimganica (see Fig. 1e); H. P. cheilanthifolia (see Fig. 1b).
FIGURE 5 in The end of a mystery: transferring Streptostachys robusta to Ichnanthus (Poaceae, Paspaleae) based on DNA sequences, morphology and leaf anatomy
FIGURE 5. Bayesian consensus tree resulting from the combined (ndhF and ITS) analysis. Bayesian posterior probabilities> 0.5 and Maximum Likelihood bootstrap support values> 50% are reported above and below branches, respectively. Ichnanthus robustus is highlighted in bold, followed by a bracket.
FIGURE 4 in The end of a mystery: transferring Streptostachys robusta to Ichnanthus (Poaceae, Paspaleae) based on DNA sequences, morphology and leaf anatomy
FIGURE 4. Part of the trees resulting from the Bayesian and Maximum Likelihood (ML) individual analyses representing the Ichnanthus clade. Bayesian posterior probabilities> 0.5 and ML bootstrap support values> 50% are reported below branches. A. ndhF Bayesian consensus tree; B. ndhF ML tree; C. ITS Bayesian consensus tree; D. ITS ML tree. Ichnanthus robustus is highlighted in bold, followed by a bracket. The accession followed by an asterisk was identified as Ichnanthus sp. BA in Silva et al. (2015b; voucher: Oliveira et al. 1216).
FIGURE 3 in The end of a mystery: transferring Streptostachys robusta to Ichnanthus (Poaceae, Paspaleae) based on DNA sequences, morphology and leaf anatomy
FIGURE 3. Stereomicroscope (SM) and scanning electron microscope (SEM) images of the upper anthecium. A–H. Ichnanthus robustus [SM: Amorim et al. 780 (CEPEC) and Silva & Daneu 1057 (HUEFS); SEM: Amorim et al. 780 (CEPEC), Borges et al. 444 (HUEFS), and Silva & Daneu 1057 (HUEFS)]. A. Young anthecium, ventral view; B. Mature anthecium, ventral view; C. Young anthecium, ventral view; D. Mature anthecium, ventral view; E. Young anthecium, base, lateral view; F. Mature anthecium, base, dorsal view; G. Mature anthecium, apex, ventral view; H. Mature anthecium, apex, lateral view. I–M. Ichnanthus bambusiflorus [SM: Ribeiro-Filho 221 (HUEFS); SEM: Silva et al. 295 (HUEFS)]. I. Young anthecium, ventral view; J. Mature anthecium, ventral view; K–M. Partially mature anthecium; K. Ventral view; L. Base, dorsal view; M. Apex, lateral view. [Scale bars A, B, I, J = 1 mm; C–H, K–M = 500 μm. GL = germination lid; L = lemma; P = palea; PB = palea base; R = rachilla; SB = silica bodies; ST = stomata; W = winged appendages]
FIGURE 1. Ichnanthus robustus. A in The end of a mystery: transferring Streptostachys robusta to Ichnanthus (Poaceae, Paspaleae) based on DNA sequences, morphology and leaf anatomy
FIGURE 1. Ichnanthus robustus. A. Habit (including inflorescence); B. Culm, leaf sheath base (node region), and leaf blade base; C. Pulvini at the base of the primary branches; D. Segment of an inflorescence branch with pairs of spikelets; E. Pair of spikelets, lateral view; F. Spikelet, dorsal view; G. Spikelet, ventral view; H–J. Young upper anthecium; H. ventral view; I. lateral view; J. dorsal view; K–M. Mature upper anthecium; K. ventral view; L. lateral view; M. dorsal view. (based on C. Silva et al. 1049)
FIGURE 6 in The end of a mystery: transferring Streptostachys robusta to Ichnanthus (Poaceae, Paspaleae) based on DNA sequences, morphology and leaf anatomy
FIGURE 6. Cross-sections of the leaf blades showing the midrib and the mesophyll of Ichnanthus robustus [Calderón et al. 2443 (CEPEC), Silva et al. 1049 (HUEFS), and Silva & Daneu 1057 (HUEFS)] and I. bambusiflorus [Silva et al. 1025 (HUEFS)]. A–D. I. robustus. A. Midrib overview; B. Mesophyll overview; C. First order vascular bundle; D. Third order vascular bundle. E–H. I. bambusiflorus. E. Midrib and mesophyll overview; F. Mesophyll, third order vascular bundles; G. First order vascular bundle; H. Third order vascular bundle. [Scale bars A–C, E = 100 μm; D, G–H = 20 μm; F = 50 μm]
FIGURE 2. Ichnanthus robustus. A in The end of a mystery: transferring Streptostachys robusta to Ichnanthus (Poaceae, Paspaleae) based on DNA sequences, morphology and leaf anatomy
FIGURE 2. Ichnanthus robustus. A. Habitat, montane forest in Southern Bahia; B. Habit; C. Base of the plant, including culms, adventitious roots, and rhizome; D. Culm, leaf sheath base (node region), and leaf blade base; E. Node region glabrous; F. Trichomes in the adaxial surface of the leaf blade; G. Vinaceous spots in the abaxial surface of the leaf blade; H. Inflorescence; I. Pair of spikelets, dorsal (left) and lateral (right) views; J. Spikelet, dorsal view. (Photos by C. Silva)
FIGURE 2 in Taxonomic transfer of the red algae Chrysymenia enteromorpha and C. wrightii to the genus Botryocladia (Rhodymeniaceae, Rhodymeniales)
FIGURE 2. Phylogram showing Botryocladia and Chrysymenia species inferred from Bayesian analysis of 22 SSU sequences, using Rhodymenia species as the outgroup taxa. Support values reflect all bootstrap values (parsimony, neighbor joining, maximum likelihood, except for Bayesian Posterior Probabilities).
FIGURE 1 in Taxonomic transfer of the red algae Chrysymenia enteromorpha and C. wrightii to the genus Botryocladia (Rhodymeniaceae, Rhodymeniales)
FIGURE 1. Phylogram inferred from RaxML analysis of 64 rbcL sequences of Rhodymeniales. The ingroup consists of 61 sequences of Rhodymeniaceae, the outgroup one representative of 3 families in the Rhodymeniales. The position of Chrysymenia enteromorpha and C. wrightii is nested inside the Botrycladia clade that includes the generitype, B. botryoides, separate from the Chrysymenia clade that includes the generitype, C. ventricosa. Numbers indicate bootstrap values at right, and BP values at left (1 represented by 100); *denotes full support. Scale bar indicates number of substitutions per site. Newly generated sequences are shown in bold.
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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)
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DANDI Archive for NWB datasets
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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.