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FIGURE 11. A in Artemisia flaccida (Asteraceae, Anthemideae) is merged with A. fulgens, with transfer of A. flaccida var. meiguensis to A. fulgens
FIGURE 11. A specimen of A. mattfeldii var. etomentosa, P.C. Tsoong 7168 (PE) from Jomda county in Xizang, misidentified as Artemisia fulgens. Inset: distal portion of stem, viscid pubescent.
FIGURE 4 in Artemisia flaccida (Asteraceae, Anthemideae) is merged with A. fulgens, with transfer of A. flaccida var. meiguensis to A. fulgens
FIGURE 4. Holotype (A) and paratype (B–D) sheets of Artemisia flaccida var. meiguensis (= A. fulgens var. meiguensis). A. China, Sichuan, Meigu county, Sichuan Chin. Trad. Med. Inst. 373 (SM). B–D. China, Sichuan, Butuo county, Sichuan Econ. Plant Exped. 1973 (KUN, PE, SM, respectively).
Monthly pCO2, gas transfer velocity and CO2 efflux rate in global streams and rivers (the GRADES river networks)
<p>The datasets contain monthly partial pressure of dissolved CO<sub>2</sub> (<em>p</em>CO<sub>2</sub>, µatm), gas transfer velocity (<em>k</em>, m d<sup>-1</sup>), and CO<sub>2</sub> efflux rate (g C m<sup>-2</sup> d<sup>-1</sup>) estimates for global streams and rivers in both comma separated values (csv) and GeoTIFF formats. These datasets served as the base for monthly CO<sub>2</sub> emission estimates for global streams and rivers and can be used to support regional terrestrial carbon balances. Original vector-version of products is based on the Global Reach–level A priori Discharge Estimates for SWOT or GRADES river networks, which have ~ 3 million individual reaches of global streams and rivers. The GeoTIFF version has a spatial resolution of approximately 0.0083º (1 km). The datasets also contain direct CO<sub>2</sub> measurements compiled from the literature (Supplementary Data 1).</p>
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.
FIGURE 10 in Research in Boraginaceae: A new variety of Cryptantha maritima, Cryptantha pondii resurrected, and Johnstonella echinosepala transferred back to Cryptantha
FIGURE 10. Cryptantha echinosepala [Johnstonella e.] distribution maps, coordinates from Baja Flora (2021). A. Topography map. Map from ©Google 2020, INEGI Data. B. Map from Baja Flora (2021) showing vegetation zones (after Rebman et al. 2016) where the species occurs.
FIGURE 2 in Research in Boraginaceae: A new variety of Cryptantha maritima, Cryptantha pondii resurrected, and Johnstonella echinosepala transferred back to Cryptantha
FIGURE 2. Distribution maps of varieties of Cryptantha maritima. Data from Baja Flora (2021), CCH2 (2021), GBIF (2020), and SEINet (2021), all specimens annotated by the authors (Appendix 1). A, B. Distribution in North America. A. Full distribution map. B. Close-up of Vizcaíno Peninsula and adjacent islands. Note location of type populations and restriction of C. maritima var. cedrosensis to Cedros Island and of C. maritima var. vizcainensis to the western Vizcaíno region. Black dots=C. maritima var. maritima; red dots=C. maritima var. pilosa; green triangles= C. maritima var. cedrosensis; yellow squares= C. maritima var. vizcainensis. C. Distribution of C. maritima var. pilosa in Argentina, South America, data from GBIF (2020). All maps from ©Google 2021, INEGI Data.
FIGURE 9 in Research in Boraginaceae: A new variety of Cryptantha maritima, Cryptantha pondii resurrected, and Johnstonella echinosepala transferred back to Cryptantha
FIGURE 9. Cryptantha echinosepala [Johnstonella e.] fruit of exemplar, León 3465, 15 March 2003 (SD153719). A. Fruit with four heteromorphic nutlets removed. Note relatively small, persistent corolla. B. Close-up of large "odd" nutlet, in dorsal (left), ventral (middle), and side (right) views. Note tuberculate-spinulose sculpturing. C. Close-up of one of the small "consimilar" nutlets, in dorsal (left), ventral (middle), and side (right) views. Note tuberculate sculpturing, lacking spinules.
FIGURE 1 in Research in Boraginaceae: A new variety of Cryptantha maritima, Cryptantha pondii resurrected, and Johnstonella echinosepala transferred back to Cryptantha
FIGURE 1. Exemplars of three varieties of Cryptantha maritima. A–C. Cryptantha m. var. maritima. A. Image of original material: Greene s.n., 26 Apr 1885, Mexico, Baja California, Guadalupe Island (UC193934). Note bracts and hispid vestiture. B. Field image, showing bracts and small corollas; photograph by Jon Rebman, 2 April 2008, Mexico, Baja California Sur, Laguna San Ignacio. C. Nutlets of fruit, one larger smooth (left) and one smaller tuberculate (right), from Simpson 2933 (SDSU19298). D, E. Cryptantha m. var. cedrosensis. D. Field image, showing larger corolla of this variety; photograph by Jon Rebman, 31 March 2015, Mexico, Baja California, Cedros Island. E. Fruiting calyx with four nutlets dissected out, these heteromorphic with one larger smooth and three smaller tuberculate; from Rebman 2446, 17 March 1994 (HCIB6234). F–H. Cryptantha m. var. pilosa. F. Field image, showing bracts, dense tufts of hirsute trichomes, and small corollas; photograph courtesy of Pablo Ruiz, United States, Pima County, Arizona, Saguaro National Park, iNaturalist observation 39812503. G, H. Images from C.V. Morton 2061, 19 March 1949 (SD113111). G. Close-up of flowers and fruits, showing calyces with dense tufts of whitish, ascending hirsute trichomes, characteristic of this variety. H. Solitary nutlet of fruit, this smooth.
FIGURE 2 in Transfer of the marine red alga Erythrocystis saccata (Rhodomelaceae, Rhodophyta) to the tribe Streblocladieae inferred from organellar genome analysis
FIGURE 2. RAxML phylogram of the complete plastid genome of Erythrocystis saccata (GenBank Accession MW810349) and representative Rhodomelaceae. Numbers along the branches are rapid bootstrap support values based on 1,000 replicates. The legend below represents the scale for nucleotide substitutions.
FIGURE 1 in Transfer of the marine red alga Erythrocystis saccata (Rhodomelaceae, Rhodophyta) to the tribe Streblocladieae inferred from organellar genome analysis
FIGURE 1. Erythrocystis saccata growing epiphytically on Laurencia pacifica from Stillwater Cove, Pebble Beach, California, USA (UC 2085026). The arrow indicates the specimen analyzed in this study. White bar = 2 cm.
FIGURE 4 in Transfer of the monospecific genus Nienburgella (Delesseriaceae, Rhodophyta) to Phycodrys, based on morphological and molecular evidence
FIGURE 4. Phycodrys radicosa (Okamura) Yamada & Inagaki from Korean coast. Vegetative morphology. A–E. Habits of female gametophyte (A, JN13102600045), tetrasprophyte (B, JN15012100001), and vegetative thalli (C, JN14091000006; D, JN14091000001; E, JN14091000003). F. Basal part of thallus. G. Multicellular rhizoids (arrowheads) along the margins of lower part of blade. H–I. Surface views of middle (H) and upper (H) parts of blade. J. Cortical cells with discoid chloroplasts. K–M. Cross-sections through lower (K), middle (L), and interveinal (M, arrow) portions of blade. N–O. Cells arrangement of blade apex with growing pattern (numbers: orders of cell rows, i: cells produced by intercalary cell division). Scale bars: C–E = 2 cm; A, B = 1 cm; F = 3 mm; I = 2 mm; H = 300 µm; G = 200 µm; K–M = 100 µm; J, N = 50 µm.
FIGURE 5 in Transfer of the monospecific genus Nienburgella (Delesseriaceae, Rhodophyta) to Phycodrys, based on morphological and molecular evidence
FIGURE 5. Phycodrys radicosa (Okamura) Yamada & Inagaki from Korean coast. Female (A–M) and tetrasporic (O–P) reproductive structures. A. Apex of marginal proliferation with procarps (arrowheads). B–G. Development process of immature procarp (cb1–3: cell numbers of carpogonial branch; cbi: carpogonial branch initial; cc: central cell; sc: supporting cell; st1: first sterile-cell group; st1i: first sterile-cell group initial; st2i: second sterile-cell group initial). H–I. Inferior (H) and superior (I) surface views of same point of mature procarp (cp: carpogonium; st2: second sterile-cell group; tr: trichogyne). J–K. Inferior (J) and superior (K) surface views of same point of post-fertilized stage (au: auxiliary cell; cbs: cells in carpogonial branch). L. Cross-section through an immature cystocarp (fu: fusion cell; gi: gonimoblast initial). M. Cross-section through a mature cystocarp. N–O. Surface views of tetrasporangial sori (t: tetrasporangia; ts: tetrasporangial sori). P. Cross-section through a tetrasporangium (ti: tetrasporangial initial). Scale bars: N = 1 mm; M, O = 100 µm; A, L, P = 50 µm; B–20 µm.
FIGURE 2 in Transfer of the monospecific genus Nienburgella (Delesseriaceae, Rhodophyta) to Phycodrys, based on morphological and molecular evidence
FIGURE 2. Nienburgella angusta (A.D. Zinova) Perestenko from the eastern coast of South Korea. Vegetative morphology. A–B Habits of tetrasporophyte (A, JN13102600046) and female gametophyte (B, JN13102600045). C. Multi-cellular rhizoids (arrowheads) along the margins of lower part of thallus. D. Surface view of middle part of main branch showing marginal rhizoids (arrowheads) and proliferation. E. Cortical cells with discoid chloroplasts. F–H. Cross-sections through apical (F), middle (G), and lower (H) part of blade. I–J. Cells arrangement of young blade with apical growing pattern (numbers: orders of cell rows, i: cells produced by intercalary cell division). Scale bars: A, B = 1 cm; C, D = 200 µm; G, H = 40 µm; E, F, I = 20 µm.
FIGURE 3 in Transfer of the monospecific genus Nienburgella (Delesseriaceae, Rhodophyta) to Phycodrys, based on morphological and molecular evidence
FIGURE 3. Nienburgella angusta (A.D. Zinova) Perestenko from the eastern coast of South Korea. Female (A–N) and tetrasporic (O–Q) reproductive structures. A–G. Development process of immature procarp (cb1–3: cell numbers of carpogonial branch; cbi: carpogonial branch initial; cbs: cells in carpogonial branch; cp: carpogonium; sc: supporting cell; st1: first sterile-cell group; st1i: first sterile-cell group initial; st2i: second sterile-cell group initial; tr: trichogyne). H. Mature procarp (st2: second sterile-cell group). I–J. Superior (I) and inferior (J) surface views of same point of post-fertilized stage (au: auxiliary cell). K–L. Cross-section through an immature cystocarp (fu: fusion cell; g: gonimoblast cell; gi: gonimoblast initial). M. Cross-section through a mature cystocarp (ca: caposporangia). N. Surface view of mature cystocarp (cs). O–P. Surface views of tetrasporangial sori (t: tetrasporangia; ts: tetrasporangial sori). Q. Cross-section through a tetrasporangium (ti: tetrasporangial initial). Scale bars: N, O = 2 mm; P = 500 µm; M, Q = 200 µm; K, L = 50 µm; A–J = 30 µm.
FIGURES 1–3 in Transfer of Homalonychus raghavai Patel & Reddy, 1991 to Storenomorpha Simon 1884 (Araneae: Zodariidae)
FIGURES 1–3. Storenomorpha raghavai (Patel & Reddy, 1991) comb. nov., original illustrations of holotype female of Homalonychus raghavai Patel & Reddy, 1991, adapted from Patel & Reddy (1991). 1 female habitus, dorsal view. 2 epigynum, ventral view. 3 vulva, dorsal view. Abbreviation: CP, central plate. Figures are not to scale.
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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.