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Distribution. Togian Archipelago (Batudaka, Togian, Talatakoh & Malenge Is); recently, their tracks also were reported from the small Kadidiri I, N of Togian I. in Suidae
Distribution. Togian Archipelago (Batudaka, Togian, Talatakoh & Malenge Is); recently, their tracks also were reported from the small Kadidiri I, N of Togian I.
Supplemental Material S2 for "Development of a highly sensitive luciferase-based reporter system to study two-step protein secretion in cyanobacteria"
<p>Table S1. Densitometric analysis of NLuc immunoblot in Fig. 2A.</p> <p>Figure S1. PilA1 quantification in the sheared pili fractions of WT, Δ<em>hfq</em> and Δ<em>pilT1</em> <em>Synechocystis</em> mutants.</p>
Subspecies and Distribution. S. J. fuscicollis Spix, 1823 — W Brazil (states of Acre & Amazonas) and Peru, S of the Rio Solimoes, between the Rio Javari in the W, E through the Rio Jutai Basin to the Rio Jurua (left bank), also in Peru, W of the Rio Yavari as far as the Rio Tapiche, an E tributary of the Rio Ucayali, and extending N from there as far as the Rio Blanco (left bank), where it meets the distribution of Geoffroy's Saddle-back Tamarin, S. nigrifrons (right bank of the Rio Blanco). S. f. auvilapiresi Hershkovitz, 1966 — W Brazil in the Amazonas State (type locality is the mouth of the Lago de Tefé, Rio Solimoes), found along the S of the Rio Solimoes between the rios Jurua and Purus, including the basins of the rios Urucu and Coari, and probably the Rio Tefé; the S limits are not known but possibly in the region of the N bank of the Rio Tapaua, an affluent of the Rio Purus. S. f. eruzlimai Hershkovitz, 1966 — W Brazil, described by Hershkovitz without provenance (based on a single individual "said to be from the upper Rio Purus"); M. G. M. van Roosmalen reported in 2003 that it had been observed by T. van Roosmalen on 21 June 2002, on the W bank of the Rio Purus, opposite the mouth of the Rio Sepatini, and noted that Hershkovitz was correct in supposing that it occurred between the rios Pauini and Tapaua, W of the Rio Purus. S. J. mura Rohe et al, 2009 — C Brazil (Amazonas State), interfluvium of the rios Madeira and Purus, S of the Rio Amazonas, probably S to the Rio Igapo-Acu. S. f. primitivus Hershkovitz, 1977 — W Brazil (Amazonas State), the distribution is believed to extend from the left bank of the Rio Pauini, along the left bank of the upper Rio Purus, N to the Rio Tapaua (right bank), as far W the right bank of the Rio Jurua, and the Rio Tarauaca. in Callitrichiade
Subspecies and Distribution. S. J. fuscicollis Spix, 1823 — W Brazil (states of Acre & Amazonas) and Peru, S of the Rio Solimoes, between the Rio Javari in the W, E through the Rio Jutai Basin to the Rio Jurua (left bank), also in Peru, W of the Rio Yavari as far as the Rio Tapiche, an E tributary of the Rio Ucayali, and extending N from there as far as the Rio Blanco (left bank), where it meets the distribution of Geoffroy's Saddle-back Tamarin, S. nigrifrons (right bank of the Rio Blanco). S. f. auvilapiresi Hershkovitz, 1966 — W Brazil in the Amazonas State (type locality is the mouth of the Lago de Tefé, Rio Solimoes), found along the S of the Rio Solimoes between the rios Jurua and Purus, including the basins of the rios Urucu and Coari, and probably the Rio Tefé; the S limits are not known but possibly in the region of the N bank of the Rio Tapaua, an affluent of the Rio Purus. S. f. eruzlimai Hershkovitz, 1966 — W Brazil, described by Hershkovitz without provenance (based on a single individual "said to be from the upper Rio Purus"); M. G. M. van Roosmalen reported in 2003 that it had been observed by T. van Roosmalen on 21 June 2002, on the W bank of the Rio Purus, opposite the mouth of the Rio Sepatini, and noted that Hershkovitz was correct in supposing that it occurred between the rios Pauini and Tapaua, W of the Rio Purus. S. J. mura Rohe et al, 2009 — C Brazil (Amazonas State), interfluvium of the rios Madeira and Purus, S of the Rio Amazonas, probably S to the Rio Igapo-Acu. S. f. primitivus Hershkovitz, 1977 — W Brazil (Amazonas State), the distribution is believed to extend from the left bank of the Rio Pauini, along the left bank of the upper Rio Purus, N to the Rio Tapaua (right bank), as far W the right bank of the Rio Jurua, and the Rio Tarauaca.
FIGURE 3 in First record of the parasitic barnacle Anelasma squalicola Darwin, 1852 (Pollicipedomorpha: Pollicipedidae) in the Eastern Pacific Ocean and a new host report: Etmopterus benchleyi Vásquez, Ebert & Long, 2015 (Squaliformes: Etmopteridae)
FIGURE 3. Anelasma squalicola (UCR 3711-001) found as parasite of the Ninja lanternshark, Etmopterus benchley. A. Specimen of ~28.8 mm TL, parasite of a female shark of 43.5 cm TL (see Fig. 1); Ovigerous specimen of ~29.1 mm TL parasite of a male shark of 52.5 cm TL (see Fig. 2); the arrowhead points towards the eggs within the mantle cavity. The peduncular bulbous structure covered with fine and root-like filaments was not properly removed from the shark tissue and, therefore, is not illustrated in the figure. Scale bar 2 cm.
FIGURE 2 in First record of the parasitic barnacle Anelasma squalicola Darwin, 1852 (Pollicipedomorpha: Pollicipedidae) in the Eastern Pacific Ocean and a new host report: Etmopterus benchleyi Vásquez, Ebert & Long, 2015 (Squaliformes: Etmopteridae)
FIGURE 2. Etmopterus benchleyi (UCR 2906-002), male (52.5 cm TL), infected by the parasitic barnacle Anelasma squalicola. A. Lateral view of the entire specimen prior to removing the parasite (Figure 3B); B. Lateral view of the entire specimen after removing the parasite; and C. Lateral view of the infected area (the basis of the left pectoral fin), prior to removing one parasite, showing a double infection. Scale bar 2 cm.
FIGURE 1 in First record of the parasitic barnacle Anelasma squalicola Darwin, 1852 (Pollicipedomorpha: Pollicipedidae) in the Eastern Pacific Ocean and a new host report: Etmopterus benchleyi Vásquez, Ebert & Long, 2015 (Squaliformes: Etmopteridae)
FIGURE 1. Etmopterus benchleyi (UCR 2906-002), female (43.5 cm TL), infected by the parasitic barnacle Anelasma squalicola. A. Lateral view of the entire specimen after removing the parasites; B. Lateral view of the infected area showing an imbibed parasite; C. Laterodorsal view of the infected area, after removing the parasite, showing a double infection. Scale bar 2 cm.
Subspecies and Distribution. L. J fons E. Geoffroy Saint-Hilaire, 1810 — Senegal and Gambia E to Nigeria, Cameroon, and Central African Republic, and S to SW Republic ofthe Congo. L.f.affinisK.Andersen&Wroughton,1907—Chad,Sudan,SouthSudan,NUganda,andextremeNEDRCongo. L. f. rex G. S. Miller, 1905 — Eritrea, Ethiopia, and Somalia S through E DR Congo, Kenya, and Tanzania (including Unguja I in Zanzibar Archipelago) to N Zambia and N Malawi. A published report from Namibia is considered an error. in Megadermatidae
Subspecies and Distribution. L. J fons E. Geoffroy Saint-Hilaire, 1810 — Senegal and Gambia E to Nigeria, Cameroon, and Central African Republic, and S to SW Republic ofthe Congo. L.f.affinisK.Andersen&Wroughton,1907—Chad,Sudan,SouthSudan,NUganda,andextremeNEDRCongo. L. f. rex G. S. Miller, 1905 — Eritrea, Ethiopia, and Somalia S through E DR Congo, Kenya, and Tanzania (including Unguja I in Zanzibar Archipelago) to N Zambia and N Malawi. A published report from Namibia is considered an error.
Figs 15–16 in Descriptions of two new African Curranosia species with characteristics not yet reported from the genus and remarks on the subspecies of Curranosia spekei s. l. (Diptera; Muscidae)
Figs 15–16: Curranosia allroundera spec. nov., holotype; 15. Left upper (uc) and lower calypter (lc); 16. Right lower calypter (lc) with the hind margin diverging from margin of scutellum (sc) almost in right angle and not extending under scutellum; (Figs 15–16, bar = 0.5 mm).
Figs 7–14 in Descriptions of two new African Curranosia species with characteristics not yet reported from the genus and remarks on the subspecies of Curranosia spekei s. l. (Diptera; Muscidae)
Figs 7–14: Curranosia allroundera spec. nov, holotype; 7. Dorsal view of female holotype; 8. Lateral view of same female but different angle of viewing, arrow pointing to shiny brown basal band, only visible when the tergite is pushed out from the overlapping posterior margin of the respective front tergite; 9. Latero-dorsal view of thorax of same specimen, shiny dark olive green only slightly dusted at different perspective; 10. Abdominal tergites brownish blue, somewhat shiny, tergite 5 consistently yellowish-brown, independent of viewing angle; 11. Right wing with brown front margin, slightly infuscate cross-vein r-m (arrow) and vein M obtusely bent towards vein R; 12. Head, lateral view, pa = palpus, pr = proboscis; 13. Head with frons in anterior view, 4+5 arrow points to anterior tip of frontal triangle; 14. Upper part of frons and frontal triangle with patches (g and arrows) consisting of microscopic golden hair; (Figs 7–11: bar = 1 mm; Figs 12 + 13: bar = 0.5 mm; Fig. 14: bar = 0.07 mm).
Figs 1–3 in Descriptions of two new African Curranosia species with characteristics not yet reported from the genus and remarks on the subspecies of Curranosia spekei s. l. (Diptera; Muscidae)
Figs 1–3: Curranosia setissima spec. nov, holotype; 1. Head, lateral view, 2. Head viewed from anterior, arrow pointing to anterior ocellus; 3. Ventral surface of wing, setula (s) and long hair-like seta (h) on the distal part of stem vein, e = end of seta, barely recognizable in the image, n = radial node. (Figs 1 and 2: bar = 0.5 mm; Fig. 3: bar = 0.2 mm.)
Open Education in European Libraries of Higher Education (2021 report dataset)
<p>In May-June 2021 SPARC Europe ran a survey among academic librarians in Europe. The survey was framed by the <a href="http://portal.unesco.org/en/ev.php-URL_ID=49556&URL_DO=DO_TOPIC&URL_SECTION=201.html">UNESCO Recommendation on OER</a>.</p> <p>Launched in May 2021, the survey, which targeted academic librarians across Europe, garnered over 230 responses from 28 countries. This data forms the basis for the<a href="https://zenodo.org/record/5734980"> 2021 report Open Education in European Libraries of Higher Education</a>.</p> <p>The survey questionnaire can be found <a href="https://zenodo.org/record/4892450">here</a>.</p> <p>The two-page summary of the key takeaways and recommendations from the report can be found here: <a href="https://zenodo.org/record/5862319">https://zenodo.org/record/5862319</a>.</p> <p>This dataset contains survey data anonymised and largely without free-text answers to ensure anonymity (.xlsx).</p> <p> </p> <p> </p> <p> </p> <p> </p> <p> </p> <p> </p>
FIGURE 13. A in New additions to the Chinese Agraeciini Redtenbacher, 1891 (Orthoptera, Tettigoniidae: Conocephalinae) with report the complete mitochondrial genome of Palaeoagraecia brunnea Ingrisch, 1998
FIGURE 13. A phylogenetic tree obtained from Bayesian inference analysis based on 13 protein-coding genes.
FIGURE 1 in New additions to the Chinese Agraeciini Redtenbacher, 1891 (Orthoptera, Tettigoniidae: Conocephalinae) with report the complete mitochondrial genome of Palaeoagraecia brunnea Ingrisch, 1998
FIGURE 1. Anelytra (Lichnofugia) symfioma (Ingrisch, 1998). Male: A. head in frontal view; B. fastigium verticis in frontal view; C–D. head and pronotum: C. dorsal view, D. lateral view; E–G. apex of abdomen: E. lateral view, F. dorsal view, G. dorso-apical view; H. subgenital plate in ventral view; I. fore left tibiae in dorsal view.
FIGURE 4 in New additions to the Chinese Agraeciini Redtenbacher, 1891 (Orthoptera, Tettigoniidae: Conocephalinae) with report the complete mitochondrial genome of Palaeoagraecia brunnea Ingrisch, 1998
FIGURE 4. Habitus of Anelytra (Lichnofugia) symfioma (Ingrisch, 1998), lateral view. A–B. male; C–D. female.
FIGURE 11. Palaeoagraecia brunnea Ingrisch, 1998 in New additions to the Chinese Agraeciini Redtenbacher, 1891 (Orthoptera, Tettigoniidae: Conocephalinae) with report the complete mitochondrial genome of Palaeoagraecia brunnea Ingrisch, 1998
FIGURE 11. Palaeoagraecia brunnea Ingrisch, 1998. Female: A. head in frontal view; B–C. head and pronotum: B. dorsal view, C. lateral view; D. processes of thoraces in ventral view; E. apex of abdomen in lateral view; G. subgenital plate in ventral view; H. apices of ovipositor in lateral view.
FIGURE 8 in New additions to the Chinese Agraeciini Redtenbacher, 1891 (Orthoptera, Tettigoniidae: Conocephalinae) with report the complete mitochondrial genome of Palaeoagraecia brunnea Ingrisch, 1998
FIGURE 8. Liara (Liara) shii Liu & Bian sp. nov. Female: A. head, pronotum and tegmina in lateral view; B–C. apex of abdomen: B. lateral view, C. dorsal view; D. fore tibiae in dorsal view; E–F. genicular lobes of hind leg: E. external view, F. internal view.
FIGURE 7 in New additions to the Chinese Agraeciini Redtenbacher, 1891 (Orthoptera, Tettigoniidae: Conocephalinae) with report the complete mitochondrial genome of Palaeoagraecia brunnea Ingrisch, 1998
FIGURE 7. Liara (Liara) shii Liu & Bian sp. nov. Female: A. head in frontal view; B. fastigium verticis in frontal view; C. head and pronotum in dorsal view; D. head, pronotum and tegmina in dorsal view; E. head and thoraces in ventral view; F. subgenital plate in ventral view.
FIGURE 3 in A new species of Podosphaera sect. Sphaerotheca subsect. Sphaerotheca from India-first report of powdery mildew causing wilting and ultimately death of leaves of Filipendula vestita
FIGURE 3. Microphotographs of fruiting bodies of Podosphaera filipendulensis (AMH 9934, holotype) a. Initial stage of developing cleistothecium (homogenious cells). b. Mature cleistothecium. c. Pseudoparenchymatous nature of wall of cleistothecium. d–g. Ruptured cleistothecia each releasing an ascus. h, i. Appendages on the surface of cleistothecia. Scale bars: a = 25 μm, b = 40 μm, c = 20 μm, d = 50 μm, e = 40 μm, f, g = 30 μm, h, i = 20 μm.
FIGURE 4 in A new species of Podosphaera sect. Sphaerotheca subsect. Sphaerotheca from India-first report of powdery mildew causing wilting and ultimately death of leaves of Filipendula vestita
FIGURE 4. Microphotographs of asci of Podosphaera filipendulensis (AMH 9934, holotype) a, b. Fully mature ascus. c, d. Ruptured asci releasing ascospores (arrows for ruptured oculi). e. Ascospores. Scale bars: a = 25 μm, b = 30 μm, c, d = 25 μm, e = 15 μm.
FIGURE 2 in A new species of Podosphaera sect. Sphaerotheca subsect. Sphaerotheca from India-first report of powdery mildew causing wilting and ultimately death of leaves of Filipendula vestita
FIGURE 2. Photographs of fruiting body of Podosphaera filipendulensis on the surface of infected leaf (AMH 9934, holotype) a. Cleistothecia (arrows) in between leaf trichomes. b–f. Cleistothecia with appendages. Scale bars: b, c = 60 μm, d = 30 μm, e = 25 μm, f = 30 μm.
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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
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.