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FIGURE 2 in Biogeographical identity of the Mesoamerican dominion with emphasis on seasonally dry tropical forests
FIGURE 2. Biogeographical regionalization and area relationships for the Neotropical region based Cluster analysis (Sorensen dissimilarity coefficient) of species of the seasonally dry tropical forests, on a grid of 0.5° × 0.5° grid-cells. Colours in the dendrogram correspond to those on the map and node labels correspond to the distance (dissimilarity) between clusters.
FIGURE 1 in A new genus of angraecoid orchids (Orchidaceae: Angraecinae) with highly distinctive pollinaria morphology, including three new species from tropical West and Central Africa
FIGURE 1. Simplified consensus tree of angraecoid genera (adapted from Simo-Droissart et al. 2018), showing the position of Kylicanthe. Bootstrap percentages and posterior probabilities are presented, respectively, above the branches. The symbol '-' indicates that the node was not retrieved in the parsimony analysis.
FIGURE 6. Kylicanthe cornuata. A. Habit. B. Inflorescence. C in A new genus of angraecoid orchids (Orchidaceae: Angraecinae) with highly distinctive pollinaria morphology, including three new species from tropical West and Central Africa
FIGURE 6. Kylicanthe cornuata. A. Habit. B. Inflorescence. C. Flower in lateral view. D. Flower in frontal view. E. Dorsal sepal. F. Lateral sepal. G. Petals. H. Lip in dorsal view. I. Column in frontal view. J. Column in lateral view. K. Column in frontal view showing rostellum. L. Anther cap. M. Pollinaria with pollinia still attached in lateral view. N. Pollinaria without pollinia in dorsal view. Drawn by Hans de Vries after Yaoundé shadehouse series 1127.
FIGURE 5. Kylicanthe bueae. A. Habit. B. Inflorescence. C in A new genus of angraecoid orchids (Orchidaceae: Angraecinae) with highly distinctive pollinaria morphology, including three new species from tropical West and Central Africa
FIGURE 5. Kylicanthe bueae. A. Habit. B. Inflorescence. C. Flower in lateral view. D. Flower in frontal view. E. Dorsal sepal. F. Lateral sepal. G. Petals. H. Lip in lateral view. I. Lip in frontal view. J. Floral pedicel, ovary and column. K. Column in lateral view. L. Column in frontal view. M. Pollinaria in dorsal view. N. Pollinaria in lateral view. Drawn by Hans de Vries after Yaoundé shadehouse series 5098 & 5958.
FIGURE 2 in A new genus of angraecoid orchids (Orchidaceae: Angraecinae) with highly distinctive pollinaria morphology, including three new species from tropical West and Central Africa
FIGURE 2. Overview of Kylicanthe diversity. A. Kylicanthe arcuata, plants growing as twig epiphytes in Mt. Etindé (Cameroon) and detail of the flowers. B. Kylicanthe perezverae, seed capsules of a plant grown at the Nimba shadehouse (Guinea). C. Kylicanthe liae, habit and detail of a flower showing a prominent orange viscidium, in cultivation at Huye orchid garden of the University of KoblenzLandau guest house (Rwanda). D. Kylicanthe bueae, habit of a plant grown at Yaoundé shadehouse (Cameroon) and detail of a flower. E. Kylicanthe quintasii, detail of inflorescence of a plant from São Tomé Island. F. Kylicanthe rohrii, detail of inflorescence of a plant from Tanzania. G. Kylicanthe cornuata, detail of flowers of a plant grown at Yaoundé shadehouse (Cameroon). Photographs by: A., D. and G. Vincent Droissart; B. Ehoarn Bidault; C. Eberhard Fischer; E. Tariq Stévart; F. W. Bachmann, facilitated by the World Orchid Iconography of the Swiss Orchid Foundation at the Herbarium Jany Renz (Botanical Institute, University of Basel, Switzerland).
FIGURE 4. Kylicanthe arcuata. A. Habit. B. Inflorescence. C. Flower. D. Dorsal sepal. E. Lateral sepal. F. Petals. G in A new genus of angraecoid orchids (Orchidaceae: Angraecinae) with highly distinctive pollinaria morphology, including three new species from tropical West and Central Africa
FIGURE 4. Kylicanthe arcuata. A. Habit. B. Inflorescence. C. Flower. D. Dorsal sepal. E. Lateral sepal. F. Petals. G. Floral pedicel, ovary and column. H. Lip in lateral view. I. Lip in dorsal view. J. Column and lip spur in frontal view showing the callus. K. Spur, detail of the mouth in dorsal view. L. Column in frontal view. M. Column in lateral view with pollinaria still attached. N. Pollinaria in lateral view. N. Anther cap in frontal view. O. Anther cap in ventral view. P. Anther cap in lateral view. Q. Pollinaria in ventral view. R. Pollinaria in lateral view showing dorsal side of stipes with pollinia still attached. S. Pollinaria in lateral view showing ventral side of stipes with pollinia still attached. Drawn by Hans de Vries after a photograph of a living specimen (A) and after Droissart & Stévart 695 (B–S).
FIGURE 1 in Phylogeny of the climber genus Haumania (Marantaceae) endemic to the tropical lowland rainforest in Central Africa
FIGURE 1. Species distribution limits (H. danckelmaniana, hatched line; H. leonardiana, dotted line; H. liebrechtsiana, hatch-dotted line) based on Dhetchuvi (1996) and localities of the collections of the three species of Haumania in Central Africa (H. danckelmaniana, black triangles; H. leonardiana, dark grey squares; H. liebrechtsiana, light grey dots). Point labels, collection numbers (Table 1). Black line, political borders.
FIGURE 2. Bayesian 50 in Phylogeny of the climber genus Haumania (Marantaceae) endemic to the tropical lowland rainforest in Central Africa
FIGURE 2. Bayesian 50% majority-rule consensus trees of the genus Haumania and major Marantaceae genera with the outgroup Canna indica (Cannaceae). Maximum Parsimony bootstrap values>70% (above branches) and posterior probabilities>0.70 (PP, below branches) are based on combined plastid dataset (matK, rps16 intron, trnL/trnL–F, trnC–petN1r) on the left and combined nuclear dataset (ITS, 5S) on the right, each including/excluding indels. Dark bold lines connecting species names from different trees indicate moderate to strong incongruencies in the tree topology between the nuclear and plastid dataset. Dashed light grey lines connect congruent taxon positions. Letters at internal tree nodes refer to clade names after Prince & Kress (2006a): A, Sarcophrynium clade; B, Stachyphrynium clade; C, Maranta clade; D, Calathea clade; E, Donax clade. Letters behind Haumania species names indicate locality of sample: C, Cameroon; G, Gabon; DRC, Democratic Republic of Congo. *, branch support is 100; -, branch support is below 0.70.
FIGURE 1 in A new species of Sidera (Hymenochaetales, Basidiomycota) from tropical Asia
FIGURE 1. Phylogeny of Sidera vesiculosa and related species generated by maximum likelihood analysis based on combined ITS and nLSU sequences. Branches are labeled with maximum likelihood bootstrap value higher than 50%, maximum parsimony bootstrap value higher than 50%, and Bayesian posterior probabilities more than 0.95.
FIGURE 4 in A new species of Sidera (Hymenochaetales, Basidiomycota) from tropical Asia
FIGURE 4. Microscopic structures of Sidera vesiculosa (holotype, BJFC025377). a: Basidiospores; b: Basidia, basidioles and cystidia; c: Hyphae from subiculum; d: Hyphae from tube trama; e: Hyphae at dissepiment edge.
FIGURE 2. A–H in Two new species of Rhodocollybia from tropical India
FIGURE 2. A–H: Rhodocollybia brevipes (CAL 1525, holotype). A & B. Basidiocarps; C. Basidiospores; D. Basidium; E. Cheilocystidia; F. Pileipellis. G. Stipitipellis; H. Terminal element of stipitipellis; I. Clamp connection on hyphae of stipitipellis. Scale bars: A-B = 10mm; C–E, H, I = 10 μm; F–G = 20 μm. Photos by K. N. Anil Raj.
FIGURE 3 in Two new species of Rhodocollybia from tropical India
FIGURE 3. ML phylogram based on nrITS sequence data showing the placement of R. ciliatomarginata and R. brevipes within the genus Rhodocollybia. Values at nodes indicate bootstrap support. BS values ≥50% are shown. Scale bar indicating the number of substitutions per site.
FIGURE 1. A–F in Two new species of Rhodocollybia from tropical India
FIGURE 1. A–F: Rhodocollybia ciliatomarginata (CAL 1244, holotype). A. Basidiocarps; B. Basidiospores; C. Basidium; D. Cheilocystidia; E. Pileipellis. F. Stipitipellis. Scale bars: A = 5mm; B–D = 10 μm; E–F = 20 μm. Photos by K. P. Deepna Latha.
TABLE 2 in Hysterium madraspatanum (Hysteriaceae), a new species from Tropical Dry Evergreen Forest of Tamil Nadu, India
<p><b>TABLE 2.</b> Comparison of morphological characteristics, hosts information of closely related species to <i>Hysterium madraspatanum</i>.</p><table><tbody><tr><th><b>S. no Species</b></th><th><b>Ascomata</b></th><th><b>Exciple</b></th><th><b>Hamathecium</b></th><th><b>Asci</b></th><th><b>Ascospores</b></th><th><b>Hosts</b></th><th><b>Reference</b></th></tr></tbody><tbody><tr><th>1.</th><td><i>H. barrianum</i></td><td>Ascomata atypically hysterithecioid, somewhat laterally compressed in the upper region, slightly connivent, sulcus very shallow, existing as a narrow rim, sides laterally striate, striae few and deep, straight to flexuous, sessile on the substrate, rarely bifurcating, taller than wide at maturity: 1–2.5 mm long × 250–450 μm high, 200–300 μm wide.</td><td>-</td><td>Pseudoparaphyses hyaline, cellular, 1–2 μm wide, branched above the ascal layer to form an epithecium.</td><td>Asci bitunicate, cylindrical, short-stipitate, (110)125– 135 × 15–20 μm.</td><td>Phragmospores fusiform, narrow, hyaline and straight when young, becoming pale-yellow to lightly clear brown, and curved when mature, highly guttulate, with guttulae large, highly refractive, present in every cell, with (7–)9(–11) septa, measuring (35–)40–45(–55) × (7–)9–10(–12) μm when mature.</td><td><i>Quercus</i></td><td>Boehm <i>et al</i>. 2009.</td></tr><tr><th>2.</th><td><i>H. insidens</i></td><td>Fruiting bodies single or in groups, embedded or erumpent, elongated, linear, tapering towards the ends, straight, not branched, up to 2.4 × 0.26 mm.</td><td>-</td><td>Pseudoparaphyses hyaline, septate, branched, with thickened tips, forming an epitheciurn above the asci.</td><td>Asci broad to cylindrical, 8 spored, irregularly biseriate, 140–150 × 18–23 μm.</td><td>Ascospores golden to dark brown, fusiform to oblong, phragmosporous, most commonly with 7 or 8 transverse septa, often <i>Salvia mellifera</i> constricted at median septum, middle cell usually swollen, 28 –35 × 10–12 μm.</td><td>E.J. van der Linde 1992.</td></tr><tr><th>3.</th><td><i>H. velloziae</i></td><td>Fruiting bodies arranged in evenly distributed groups, embedded or erumpent, broad to ellipsoid with almost abrupt ends, slit broad, straight, not branched, up to 1.2 × 0.5 mm.</td><td>-</td><td>Pseudoparaphyses hyaline, septate, filiform, not thickened much at the tips, branched to form an epithecium.</td><td>Asci irregularly biseriate, broad cylindrical, 8 spored, 130–140 × 20–25 μm.</td><td>Ascospores light brown with dark brown septa, fusiform, phragmosporous, 13–21 septate, most commonly 14 or 15 septate, 45–50(60) × 10–12 (14) μm.</td><td>-</td><td>E.J. van der Linde 1992.</td></tr><tr><th>4.</th><td><i>H. angustatum</i></td><td>Hysterothecia superficial with base immersed, carbonaceous, black, subglobose to elongate, straight or flexuous, smooth laterally, with a longitudinal slit, sulcus shallow, gregarious, lying at irregular angles, without KOH Extractable pigment 0.2–1.4 × 0.1–0.3 mm, 0.1–0.3 mm high.</td><td>-</td><td>Pseudoparaphyses Asci bitunicate, cylindrical, septate, hyaline, branched short pedicillate, 8 spored, above the asci, 1–1.5 µm irregularly biseriate, wide. 57.5–88 × 9–11 µm.</td><td>Ascospores 16–30 x 4–8.5 µm, 3- septate (rarely 4-septate), narrowly ellipsoidal-ovoid to cylindrical with rounded ends, often with one side straight, reddish brown, slightly constricted at the septa, the end cells concolorous or slightly paler than median cells.</td><td><i>Platanus occidentalis, Corylus avellana, Betula pendula, Prunus spinosa, Fraxinus excelsior.</i></td><td>Jayasiri S. C. <i>et al</i>. 2018.</td></tr><tr><th>5.</th><td><i>H. citricola</i></td><td>Ascocarps superficial elongated stromatic, The wall lined by black hard and opening by narrow long slit thick walled cells. measuring from 1537–1762 × 450 –787 µm.</td><td>Paraphyses occasionally branching forming the epithecium at apex</td><td>Asci hyaline to slightly yellow in colour, arises from the basal hymenium layer which are parallel, bitunicate, cylindrical to clavate, 8 spored measuring from 118–170 × 9–11 µm.</td><td>Ascospores uniseriately arranged, 4 celled, hyaline first later changing to yellow and then dark brown, <i>Citri limon</i> oblong to ellipsoid measuring from 20–26 × 7–8 µm.</td><td>Tilak <i>et al</i>. 1966</td></tr><tr><th>6.</th><td><i>H. lantanae</i></td><td>Ascocarp superficial elongated stromatic, black and hard and opening by narrow long slit measuring from 1300–1470 × 450 –525 µm from the basal hymenium layer.</td><td>The wall lined by thick walled cells.</td><td>Paraphysate, paraphyses occasionally branched forming the epithecium at apex.</td><td>From the basal hymenium layer asci originate which are parallel, bitunicate, cylindrical to clavate, 8 spored measuring from 125–145 × 7–11 µm, hyaline to slightly yellow in colour.</td><td>Ascospores uniseriately arranged, initially two celled and finally four celled, hyaline first, later changing <i>Lantana camara</i> to yellow and then dark brown, oblong to ellipsoid, measuring from 24–30 × 8–9.6 µm.</td><td>Tilak <i>et al</i>. 1966.</td></tr><tr><th>7.</th><td><i>H. tamarindi</i></td><td>Ascocarp superficial elongated stromatic black hard and opening by narrow long slit measuring from 700–1560 × 285–435 µm.</td><td>The wall lined by thick walled cells.</td><td>Paraphyses occasionally branching, forming the epithecium at the apex.</td><td>From the basal hymenium layer asci originate which are parallel, bitunicate, cylindrical to clavate 8 spored measuring from 156–210 × 9–11 µm, hyaline to slightly yellow in colour,</td><td>Ascospores uniseriately arranged, initially two celled which ultimately become four celled, hyaline first, later changing to yellow and then dark brown, oblong to ellipsoid, measuring from 19–30 × 7–8 µm.</td><td><i>Tamarindus indica</i></td><td>Tilak <i>et al</i>. 1966.</td></tr><tr><th>8.</th><td><i>H. memecyli</i></td><td>Ascocarps superficial elongated stromatic, black hard and, opening by narrow long slit, measuring from 700–900 × 450–550 µm.</td><td>The wall lined by thick walled cells.</td><td>Paraphyses occasionally branching, forming the epithecium at apex.</td><td>From the basal hymenium layer asci originate which are parallel, bitunicate, cylindrical to clavate, 8 spored measuring from 200–240 × 8–11 µm, hyaline to slightly yellow in colour.</td><td>Ascospores uniseriately arranged, initially two celled and finally become four celled, hyaline first, later changing to yellow and then dark brown, oblong to ellipsoid, measuring from 29–32 × 7–9 µm.</td><td><i>Memecylon edule</i></td><td>Tilak <i>et al</i>. 1966.</td></tr><tr><th>9.</th><td><i>H. celastrinum</i></td><td>Ascocarps superficial elongated stromatic, black hard and opening by narrow long slit measuring from 350–750 × 150–250 µm.</td><td>The wall is lined by thick walled cells and measures from 20–30 × 8 –12 µm.</td><td>Paraphyses occasionally branching, forming the epithecium at apex.</td><td>From the basal hymenium layer originate asci which are parallel, bitunicate cylindrical to ctavate 8 spored, measuring from 60–75 × 5–6 µm, hyaline to slightly yellow in colour.</td><td>Ascospores uniseriately arranged. 4 celled, hyaline first later changing to yellow and then dark brown, oblong to ellipsoid, measuring from 26.1– 29 × 5.8–9 µm.</td><td><i>Celastrus paniculatus</i></td><td>Tilak 1963.</td></tr><tr><th>10.</th><td><i>H. hyalinum</i></td><td>Asomata hysteriaceous, i.e they are elongate with a central narrow fissure, black, carbonaceous and remain closed when wet.</td><td>-</td><td>-</td><td>The asci of the species measures 95–110 × 15 µm.</td><td>Ascospores become pale brown when matured, occasionally, they are 4 or 5 septate.</td><td><i>Populus</i></td><td>Cooke <i>et al</i>. 1875.</td></tr><tr><th>11.</th><td><i>H. pulicare</i></td><td>Ascostromata 500–2000 × 300–500(–700) µm, 200–300 µm tall, erumpent through bark Peridium with lateral or appearing superficial on wood where the walls 50–90 µm thick, bark is lost, elongate, narrowly elliptical to composed of very fusiform in outline, straight or irregularly dark, near opaque, curved, ovate to doliiform in vertical thick walled brown section, constricted at the base, scattered to black cells, basal or gregarious, superficial or nearly so, dull region similar, with a black, with a conspicuous longitudinal layer of hyaline thin cleft and often with inconspicuous parallel walled cells 40–50 striations, the cleft gradually widening to µm thick forming the expose the hymenium, which is coloured cavity floor. dark brown by the ascospores and encrusted paraphysoids.</td><td>Interascal tissue of paraphysoids <i>ca</i> 1.5 µm diam, filiform with rounded ends, hyaline, smooth, sparsely septate, branched and sometimes anastomosed, exceeding the asci and plugging the ascomatal slit when dry, occasionally with slight apical encrustation where exposed.</td><td>Asci (75–) 100–120 × 17–24 µm, cylindrical-clavate, stalked, tapering to a rounded or irregular base, thick-walled, fissitunicate, apex rounded, 8 spored, arising in parallel from the cavity floor.</td><td>Ascospores 26–37 × 7–12 µm, 3 septate (very rarely 4 septate), end cells much paler (near-hyaline), narrowly ellipsoidal-ovoid to cylindrical with rounded ends, often with one side straight, reddish brown, slightly constricted at the septa, the end cells concolorous or slightly paler than median cells.</td><td>Quercus</td><td>Boehm <i>et al</i>. 2009.</td></tr><tr><th>12.</th><td><i>H. petiolare</i></td><td>Hysterothecia 0.5 –1.0 × 0.2–0.4 mm, separate and in subparallel rows, ostiole prominent, frequently with a distinct rim surrounding its base giving a hat-shaped appearance to the fructification.</td><td>-</td><td>-</td><td>-</td><td>spores hyaline, filiform, non-septate, 40–55 × 1.5 µm.</td><td><i>Rhus glabra and Quercus</i></td><td>Lowy B 1949.</td></tr><tr><th>13.</th><td><i>H. rhizophorae</i></td><td>Peridium 25–75 (x Saprobic on decaying wood of Ascomata = 50 μm, n = 5)μm hysterothecial, 650–2100 μm long (x = 1060 wide, carbonaceous, μm, n = 5), 100–400 μm high, 170–200 μm comprising an outer wide (x = 243 × 199 μm, n = 5), erumpent layer of dark brown to superficial with base immersed, solitary cells of textura to gregarious, straight to flexuous, ellipsoid globosa and aninner or elongate, with pointed ends, opening by a layer of hyaline to depressed longitudinal slit, invertical section pale brown cells of sub-globose to globose, carbonaceous, black. textura globosa.</td><td>Ascospores 10–17 × 3–5 μm (x = 14 × 4 μm, n = 30), overlapping Pseudoparaphyses Asci 40–65 × 6–12 μm (x = biseriate, light brown, ellipsoidal, 1–2 μm (n = 30) wide, 48 × 10 μm, n = 20),8 spored, straight to slightly curved, with cellular, septate, flexuous, bitunicate, cylindric to 3 transverse septa, often slightly branched. claviform, short pedicellate. constricted at the median septum, with or without guttules.</td><td><i>Rhizophora apiculata</i> and <i>Aegiceras corniculatum</i></td><td>Devdatha <i>et al</i>. 2018</td></tr><tr><th>14.</th><td><i>H. calabash</i></td><td>Apothecia gregarious in little clusters on the substratum, straight or curved, reaching a length of 1 mm.</td><td>-</td><td>-</td><td>Asci clavate, reaching a length of 70 μm and a diameter of 10 μm.</td><td>8 spored; spores fusoid, 3 septate, slightly constricted at the septa, pale-brown, about 18 × 8 μm.</td><td><i>Crescentia cujete</i> and <i>Lagenaria siceraria</i></td><td>Seaver, F. J. 1924.</td></tr></tbody></table><p>......continued on the next page</p><p>......continued on the next page</p>
Database of upper ocean mixing enhanced by tropical cyclones in the northern South China Sea in 2023
<p>Data reported in the manuscript "Identification and quantification of upper ocean mixing enhanced by tropical cyclones in the northern South China Sea" can be downloaded here.</p> <p>Matlab (versions later than 9.12.0.1884302 (R2022a)) is necessary to run the postprocessing codes.</p>
Table 1 in Revision of the tropical genus Diplacrum (Cyperaceae: Bisboeckelereae) in Australia
<p>Table 1. Currently recognised species of <i>Diplacrum</i>.</p><table><thead><tr><th>Current name</th><th>Distribution</th><th>Descriptions</th></tr></thead><tbody><tr><th><i>D. africanum</i> (Benth.) C.B.Clarke</th><td>Tropical Africa, Madagascar, southern India, and in Suriname (possibly introduced; see Koyama and Oldenburger 1971)</td><td>Napper (1964) *, Haines and Lye (1983) *, Prasad and Singh (2002) *, Samain and Goetghebeur (2006), Hoenselaar <i>et al</i>. (2010) *, Dey and Prasaana (2015), Browning and Goetghebeur (2017) *, Browning <i>et al</i>. (2020) *, Lebrun and Stork (2020)</td></tr><tr><th><i>D. blakei</i> K.L.Wilson & R.L.Barrett</th><td>Northern Australia</td><td>This paper*</td></tr><tr><th><i>D. capitatum</i> (Willd.) Boeckeler</th><td>Tropical Americas, western and western–central tropical Africa</td><td>Adams (1972), Koyama (1979 <i>b</i>) *, Kearns (1998) *, GÓmezLaurito (2003), Lye and Thery (2012) *, Mesterházy (2012) *, Lebrun and Stork (2020)</td></tr><tr><th><i>D. caricinum</i> R.Br.</th><td>India and Sri Lanka to Japan, Malesia and Australia</td><td>Kern (1961 <i>a</i>, 1974)*, Walker (1976), Koyama (1964, 1985), Hô (1993), Noltie (1994) *, Simpson and Koyama (1998) *, Koyama <i>et al</i>. (2000), Prasad and Singh (2002) *, Zhang <i>et al.</i> (2010) *, Dey and Prasaana (2015), Simpson (2019) *, this paper*</td></tr><tr><th><i>D. exiguum</i> (J.Kern) T.Koyama</th><td>Vietnam</td><td>Kern (1962) *</td></tr><tr><th><i>D. guianense</i> (Nees) T.Koyama</th><td>Northern South America</td><td>Maguire (1967), Kearns (1998) *</td></tr><tr><th><i>D. latzii</i> K.L.Wilson & R.L.Barrett</th><td>Northern Australia</td><td>This paper*</td></tr><tr><th><i>D. mitracarpoides</i> (Standley & L.O.Williams) C.D.Adams</th><td>Honduras</td><td>Standley and Williams (1952), Adams (1994)</td></tr><tr><th><i>D. poklei</i> (Wad.Khan) K.C.Mohan</th><td>Southern India</td><td>Wadoodkhan <i>et al.</i> (2007), Wadoodkhan (1999, 2014)*, Dey and Prasaana (2015) *, Chandramohan <i>et al</i>. (2016, 2020)*</td></tr><tr><th><i>D. pygmaeopsis</i> (Kern) T.Koyama</th><td>Indonesia (Lesser Sunda Islands)</td><td>Kern (1961 <i>a</i>, 1974)*</td></tr><tr><th><i>D. pygmaeum</i> (R.Br.) Nees ex Boeckeler</th><td>Northern Australia</td><td>Kern (1961 <i>a</i>) *, Rye (1992), this paper*</td></tr><tr><th><i>D. reticulatum</i> Holtt.</th><td>Bangladesh to Hainan and Peninsular Malaysia</td><td>Holttum (1947) *, Zhang <i>et al.</i> (2010)</td></tr></tbody></table><p>Note that species listed here are commonly treated under <i>Scleria</i> in the references cited. Asterisks (*) indicate that illustrations are included.</p>
Data for article BFT-Assekoetal2024_diffusion_of_tropical_hardwoods
<p>This dataset contains Excel sheets of the measurements concerning the work presented in the article "Diffusion properties of Gabonese tropical hardwoods and European<br>softwoods measured with low-tech equipment and by an inverse method" in <em>Bois et Forêts des Tropiques </em>journal. It also contains python script used for the analysis that allowed to estimate the diffusion parameters with an inverse method.</p>
Ontogenetic Shifts in Behavior and Host-Plant Preference of a Tropical Clown Grasshopper
<p>This repository contains all the data and scripts necessary to perform the analyses of the study</p>
FIGURE 2. Calyptocarpus vialis Less. A in Calyptocarpus (Asteraceae: Heliantheae: Ecliptinae), a newly naturalized genus in Tropical East Africa
FIGURE 2. Calyptocarpus vialis Less. A. Habit; B. Capitulum; C. Ray floret; D. Disc floret with palea; E. Achenes; F. Corolla; G. Anther; H. Floret showing style branches.
FIGURE 1 in Calyptocarpus (Asteraceae: Heliantheae: Ecliptinae), a newly naturalized genus in Tropical East Africa
FIGURE 1. Cladogram of the maximum likelihood (ML) phylogenetic tree based on combined data (ITS & ETS). Numbers near the nodes represent Ultrafast bootstrap values (UBS). Boldface letter indicated newly added sequence.
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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)
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
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