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243 results for “new varieties”
FIGURE 1 in Three new species of Crinipellis and one new variety of Moniliophthora (Basidiomycota, Marasmiaceae) described from the Republic of Korea
FIGURE 1. Photos of basidiocarps. A-a. Crinipellis birhizomorpha, A-b. two types of rhizomorphs of C. birhizomorpha, B. C. wandoensis, C-a. C. pallidipilus, C-b. one type of rhizomorph of C. pallidipilus, d. Moniliophthora conchata var. brevispora. Photo V. Antonín and K.-H. Ka.
FIGURE 5. Moniliophthora conchata var. brevispora. a. cheilocystidia, b. basidiospores, c in Three new species of Crinipellis and one new variety of Moniliophthora (Basidiomycota, Marasmiaceae) described from the Republic of Korea
FIGURE 5. Moniliophthora conchata var. brevispora. a. cheilocystidia, b. basidiospores, c. pileus hairs. Scale bar = 20 μm.
FIGURE 3. Crinipellis wandoensis. a. cheilocystidia, b. basidiospores, c in Three new species of Crinipellis and one new variety of Moniliophthora (Basidiomycota, Marasmiaceae) described from the Republic of Korea
FIGURE 3. Crinipellis wandoensis. a. cheilocystidia, b. basidiospores, c. pileus hairs. Scale bar = 20 μm.
FIGURE 7 in Three new species of Crinipellis and one new variety of Moniliophthora (Basidiomycota, Marasmiaceae) described from the Republic of Korea
FIGURE 7. Phylogenetic tree of the genus Crinipellis based on LSU rDNA using Bayesian (MCMC) and Maximum likelihood (ML) analysis. The phylogenetic tree is a 50% majority-rule consensus tree using GTR + G model with 107 generations for four chains and calculated from the burn-in value of 25,000 trees on MCMC analysis. This tree is estimated in 1000 replicates with the random addition of sequences during each heuristic search under ML analysis. The numbers on the left are posterior probabilities (PP) and those on the right are bootstrap values (BS) on the supported node of the phylogenetic tree.
FIGURE 6 in Three new species of Crinipellis and one new variety of Moniliophthora (Basidiomycota, Marasmiaceae) described from the Republic of Korea
FIGURE 6. Phylogenetic tree of the genus Crinipellis based on ITS rDNA using Bayesian (MCMC) and Maximum likelihood (ML) analyses. The numbers on the left are posterior probabilities (PP) and those on the right are bootstrap values (BS) on the supported node. The phylogenetic tree is a 50% majority-rule consensus tree calculated from the burn-in value of 25,000 trees using the GTR + G model with 107 generations for four chains on MCMC analysis, and estimated in 1000 replicates with the random addition of sequences during each heuristic search under ML analysis.
FIGURE 2. Crinipellis birhizomorpha. a. cheilocystidia, b. basidiospores, c. pileus hairs, d in Three new species of Crinipellis and one new variety of Moniliophthora (Basidiomycota, Marasmiaceae) described from the Republic of Korea
FIGURE 2. Crinipellis birhizomorpha. a. cheilocystidia, b. basidiospores, c. pileus hairs, d. surface of abortive pilei. Scale bar = 20 μm for a–c, 50 μm for d.
FIGURE 1. Musa balbisiana var. elavazhai. A. habit. B in A new variety of Musa balbisiana Colla (Musaceae) from South India
FIGURE 1. Musa balbisiana var. elavazhai. A. habit. B. pseudostem color at young stage. C. color at maturity. D. leaf apex. E. leaf base. F. cross-section of petiole, G. inflorescence at emerging stage. H–M. female flower parts. H. entire flower. I–J compound tepal. K. flower without tepals. L. free tepal. M. cross-section of ovary. N–O. bract. P–Q. male flower parts. P. entire flower. Q. flower without tepals. R. inflorescene at advanced blooming. S. fruit bunch. T. single fruit. U. seeds. Photos by Alfred Joe.
FIGURE 1 in On the occurrence of a new variety of Amomum villosum (Family Zingiberaceae) in Central Hills of Sri Lanka
FIGURE 1. Illustration of Amomum villosum var. zeylanicus Karunarathne and Yakandawala, A. Peduncle bearing mature fruits, B. Mature inflorescence, C. Dissected flower showing epigynous glands and style, D. Mature flower, E. Labellum, F. Peduncle sheath, G. Bract, H. Bracteole, I. Calyx, J. Stigma, K. Anther with the crest, L. CS of a mature fruit, M. Leaf showing venation and attachment of the leaf to the stem, N. Ventral view of a ligule and leaf petiole, O. Ligule.
FIGURE 2 in Crepidomanes inopinatum var. tamonii (Hymenophyllaceae), a new lowland variety endemic to semi-dry forests in La Réunion
FIGURE 2. Crepidomanes inopinatum var. tamonii. In situ epilithic colony covering a wet rock in a ravine in La Réunion semi-dry forest, 'La Grande Chaloupe' locality (photograph by Y. Robert).
FIGURE 3. Crepidomanes inopinatum. A in Crepidomanes inopinatum var. tamonii (Hymenophyllaceae), a new lowland variety endemic to semi-dry forests in La Réunion
FIGURE 3. Crepidomanes inopinatum. A. Typical large form occurring in mountainous rainforest (E. Grangaud 1184-1, collected at 'Rivière des Marsouins, Forêt de Bébour', 1,320 m). B. Dwarf fertile forms occurring in lowland to midland semi-dry forest (Y. Robert 885, 'Sentier Piton Petit Louis, Grand Bassin', 900 m) and corresponding to C. inopinatum var. tamonii. Scale = 1 cm.
FIGURE 1 in Crepidomanes inopinatum var. tamonii (Hymenophyllaceae), a new lowland variety endemic to semi-dry forests in La Réunion
FIGURE 1. Localization of the Mascarene Archipelago or Mascarenes in the Indian Ocean (left) and collection localities (white polygons) for Crepidomanes inopinatum var. tamonii in La Réunion (right).
FIGURE 3 in Taxonomic updates and a new variety of Cosmarium redimitum from South America
FIGURE 3. Updated distribution of Cosmarium redimitum in South America. 1—Borge 1899; 2—Thérézien 1985; 3—Oliveira 2000; 4— Coesel 1992; 5—Duque et al. 2013; 6—Salazar & Guarrera 2000; 7—Couté & Tell 1981; 8—Borge 1925; 9—Grönblad 1945; 10—Förster 1964; 11—Förster 1969; 12—Thomasson 1971; 13—Sophia & Dias 1996; 14—Pereira 2011; 15—Bicudo et al. 2019; 16—Saturtino et al. 2020; * New records from Bahia.
FIGURE 2 in Taxonomic updates and a new variety of Cosmarium redimitum from South America
FIGURE 2. Cosmarium redimitum var. acroscrobiculatum var. nov. (SEM). A–B. Frontal view C. Cell division F. Cell wall details; white arrowheads—flattened tubercles; yellow arrowheads—scrobicles. E. Apical view.
FIGURE 1 in Taxonomic updates and a new variety of Cosmarium redimitum from South America
FIGURE 1. Cosmarium redimitum var. acroscrobiculatum var. nov. (LM). A–D. Frontal view E. Apical view; arrowheads—scrobicles. F. Cell division G. Zygospore; arrowheads—elongated tubercles of the mother cell.
FIGURE 8 in Research in Boraginaceae: A new variety of Cryptantha maritima, Cryptantha pondii resurrected, and Johnstonella echinosepala transferred back to Cryptantha
FIGURE 8. Cryptantha echinosepala [Johnstonella e.] A. Holotype (Orcutt 15, March 1917, GH00096294), close-up of one plant. Note occasional bracts at base of inflorescence cymules and scattered flower bracts. B-D. Exemplar specimen, Carter 3894, 20 March 1960 (SD106211). B. Stem close-up, showing in this specimen appressed-strigose trichomes. C. Basal leaf close-up, showing marginal pustulate, hispid trichomes. D. Fruit close-ups, showing characteristic hispid trichomes of calyx concentrated on the axial (upper/toward inflorescence axis) side.
FIGURE 7. A,B in Research in Boraginaceae: A new variety of Cryptantha maritima, Cryptantha pondii resurrected, and Johnstonella echinosepala transferred back to Cryptantha
FIGURE 7. A,B. Cryptantha pondii, distribution map of three known collections. Georeference point for the type, Pond 22, approximate; that of Gentry 8684 placed as a centroid of three different georeferenced estimates. Maps from ©Google 2020, INEGI Data.
FIGURE 3. Cryptantha maritima var. vizcainensis. Images from Moran 19878 in Research in Boraginaceae: A new variety of Cryptantha maritima, Cryptantha pondii resurrected, and Johnstonella echinosepala transferred back to Cryptantha
FIGURE 3. Cryptantha maritima var. vizcainensis. Images from Moran 19878 (SD92358). A. Close-up of base of primary shoot, showing strigose stem vestiture and pustulate trichomes of leaves. B. Corolla face, showing relatively large limb diameter and fornices. C. Mature fruit, calyx opened, showing two nutlets and style, extending just beyond larger, smooth nutlet. D. Close-up of cymule, showing appressedstrigose stem vestiture, flower bract, calyces with hirsute marginal regions of ascending trichomes, and hispid midribs with stout, inclined or spreading trichomes, the latter more prominent on the side away from the inflorescence axis.
FIGURE 6. Cryptantha pondii. A in Research in Boraginaceae: A new variety of Cryptantha maritima, Cryptantha pondii resurrected, and Johnstonella echinosepala transferred back to Cryptantha
FIGURE 6. Cryptantha pondii. A. Close-up of single plant of presumed lectotype specimen (US41006), confirmed by Johnston (1928) as being correctly identified. Note linear, pustulate leaves and bracts at base of cymules. B,C. Images from Gentry 8684, 13 March 1949 (HCIB21969). B. Four nutlets removed from fruit, showing smooth surface and slight size heteromorphism. C. Close-up of cymules, showing linear bracts and relatively large corollas. D–F. Images from Philbrick B74-84, 25 March 1974 (SBBG49613). D. Fruit with four, smooth nutlets removed. Note finely hirsute calyx marginal region with ascending trichomes, as well as hispid calyx midrib of stouter trichomes. E. Close-up of four nutlets attached to gynobase. Note slight heteromorphism in size and slight extension of style tip/stigma from nutlet apices. F. Cymules, showing appressed-strigose vestiture of axes, scattered linear flower bracts, and relatively large corolla.
FIGURE 5 in Research in Boraginaceae: A new variety of Cryptantha maritima, Cryptantha pondii resurrected, and Johnstonella echinosepala transferred back to Cryptantha
FIGURE 5. Comparisons of fruiting calyces of Cryptantha maritima varieties. A. Cryptantha maritima varieties, left-to-right: var. cedrosensis, var. maritima, var. pilosa, and var. vizcainensis. B. Two samples of var. maritima; note hirsute calyx margin region with few to many appressed trichomes and hispid calyx midrib with stout, mostly spreading trichomes. C. Two samples of var. pilosa; note densely hirsute calyx margin region with ascending to erect trichomes and hispid midribs with few, relatively thin, erect to ascending trichomes.
FIGURE 4. Cryptantha maritima var. vizcainensis. Images from Moran 19878 in Research in Boraginaceae: A new variety of Cryptantha maritima, Cryptantha pondii resurrected, and Johnstonella echinosepala transferred back to Cryptantha
FIGURE 4. Cryptantha maritima var. vizcainensis. Images from Moran 19878 (SD92358). A. Gynobase, nutlets, and style/stigma detached from a single fruit. B. Larger, smooth nutlet, in dorsal (left) and ventral (right) views. C. Smaller, tuberculate nutlet, in dorsal (left) and ventral (right) views. Note ventral groove, short bifid at base.
ScienceDex guides
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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.