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Figure 7 in A new species of Paratrigona Schwarz, 1938 from northeastern Brazil, with notes on the type material of Melipona lineata Lepeletier, 1836 (Hymenoptera: Anthophila: Apidae)
Figure 7. Holotype of Paratrigona incerta Camargo & Moure, 1994, deposited at the Prof. J.M.F. Camargo Collection from the RPSP, University of São Paulo, Ribeirão Preto, Brazil: (a). Frontal view of head; (b). Lateral view of body; (c). Lateral view of mesepisternum; (d). Dorsal view of mesosoma; (e). Labels. Arrows indicate presence or absence of setae. Ownership rights to these images and their copyright belong to RPSP (Coleção Entomológica 'Prof. J.M.F. Camargo'). Photo by E.A.B. Almeida.
Figure 3 in A new species of Paratrigona Schwarz, 1938 from northeastern Brazil, with notes on the type material of Melipona lineata Lepeletier, 1836 (Hymenoptera: Anthophila: Apidae)
Figure 3. Lectotype of Melipona lineata Lepeletier, 1836 deposited at the MNHP, Paris, France: (a). Frontal view of head; (b). Lateral view of body; (c, d). Dorsolateral view of mesoscutum and mesoscutellum; (e). Metatibia; (f). Labels of lectotype. Arrows indicate presence of setae.
Figure 4 in A new species of Paratrigona Schwarz, 1938 from northeastern Brazil, with notes on the type material of Melipona lineata Lepeletier, 1836 (Hymenoptera: Anthophila: Apidae)
Figure 4. Paralectotype of Melipona lineata Lepeletier, 1836 deposited at the MNHP, Paris, France: (a). Frontal view of head; (b). Lateral view of head; (c). Lateral view of body; (d). Dorsolateral view of mesosoma; (e). Metatibia; (f). Labels of paralectotype. Arrows indicate absence of setae.
Figure 1 in A new species of Paratrigona Schwarz, 1938 from northeastern Brazil, with notes on the type material of Melipona lineata Lepeletier, 1836 (Hymenoptera: Anthophila: Apidae)
Figure 1. Holotype female (worker) of Paratrigona intermedia Oliveira, Madella-Auricchio & Freitas sp. nov., deposited at the MHNBA, Salvador, Bahia State, Brazil: (a). Frontal view of head; (b). Lateral view of body; (c). Mesepisternum in profile, and iridescence on wing; (d). Dorsolateral view of mesoscutum and mesoscutellum. Arrows indicate presence or absence of setae.
Figure 2 in A new species of Paratrigona Schwarz, 1938 from northeastern Brazil, with notes on the type material of Melipona lineata Lepeletier, 1836 (Hymenoptera: Anthophila: Apidae)
Figure 2. Holotype female of Paratrigona intermedia Oliveira, Madella-Auricchio & Freitas sp. nov., deposited at the MHNBA, Salvador, Bahia State, Brazil: (a). Mesepisternum in profile; (b). Metatibia; (c). Labels. Arrow indicates whitish setae/pilosity.
FIGURE. Phylogenetic tree based on RAxML analyses of a combined LSU, ITS and SSU dataset. Bootstrap support values for ML and MP equal to or greater than 75% and PP value greater than 0.95 are in thickened. Ex-type isolates are in bold, and new taxa are indicated in red. The tree is rooted with Atractospora aquatica (S-1297) and A. aquatica (MFLU 18–2322). in Conlarium sichuanense sp. nov., on Ficus virens from Sichuan Province, China
FIGURE. Phylogenetic tree based on RAxML analyses of a combined LSU, ITS and SSU dataset. Bootstrap support values for ML and MP equal to or greater than 75% and PP value greater than 0.95 are in thickened. Ex-type isolates are in bold, and new taxa are indicated in red. The tree is rooted with Atractospora aquatica (S-1297) and A. aquatica (MFLU 18–2322).
Thermal Equations of State of Corundum and Rh2O3 (II)-type Al2O3 up to 153 GPa and 3400 K
<p>Supporting information for the article "<strong>Thermal Equations of State of Corundum and Rh<sub>2</sub>O<sub>3</sub> (II)-type Al<sub>2</sub>O<sub>3</sub></strong> <strong>up to 153 GPa and 3400 K</strong>"</p>
Molecular Dynamics of HLA-A 02:01 with neoantigen and wild-type peptides from AKP6 and ASTN1 genes.
<p>Molecular Dynamics simulations of 4 complexes :</p> <p>1. Protein HLA-A*02:01 with the wild-type peptide WLIDMESLV from AKP6 gene.</p> <p>2. Protein HLA-A*02:01 with the neoantigen peptide WLIDMKSLV from AKP6 gene.</p> <p>3. Protein HLA-A*02:01 with the neoantigen peptide KLYGLDWAEL from ASTN1 gene.</p> <p>4. Protein HLA-A*02:01 with the wild-type peptide KPYGLDWAEL from ASTN1 gene.</p>
Phytolith-occluded carbon sequestration potential in three major steppe types along a precipitation gradient in Northern China
<p>Phytolith-occluded carbon (PhytOC) is an important long-term stable carbon fraction in grassland ecosystems, and plays a promising role in global carbon sequestration. Determination of the PhytOC traits of different plants in major grassland types is crucial for precisely assessing their phytolith carbon sequestration potential. Precipitation is the predominant factor in controlling net primary productivity (NPP) and species composition of the semiarid steppe grasslands. We selected three representative steppe communities of the desert steppe, the dry typical steppe and the wet typical steppe in Northern Grasslands of China along a precipitation gradient, to investigate their species composition, biomass production and PhytOC content for quantifying its long-term carbon sequestration potential. Our results showed that (i) the phytolith and PhytOC contents in plants differed significantly among species, with dominant grass and sedge species having relatively high contents, and the contents are significantly higher in the below- than the aboveground parts. (ii) The phytolith contents of plant communities were 16.68, 17.94 and 15.85 g kg<sup><span>-1</span></sup> in the above- and 86.44, 58.73 and 76.94 g kg<sup><span>-1</span></sup> in the belowground biomass of the desert steppe, the dry typical steppe and the wet typical steppe, respectively; and the PhytOC contents were 0.68, 0.48 and 0.59 g kg<sup><span>-1</span></sup> in the above- and 1.11, 0.72 and 1.02 g kg<sup><span>-1</span></sup> in the belowground biomass of the three steppe types. (iii) Climatic factors affected phytolith and PhytOC production fluxes of steppe communities mainly through altering plant production, whereas their effects on phytolith and PhytOC contents were relatively small. Our study provides more evidence on the importance of incorporating belowground PhytOC production for estimating phytolith carbon sequestration potential, and suggests it crucial to quantify belowground PhytOC production taking into account of plant perenniality and PhytOC deposition over multiple years.</p>
FIGURE 6 in Jurodidae (Coleoptera: Archostemata) from Transbaikalia: new findings and redescription of type material
FIGURE 6. Jurodes shef sp. nov. A, Holotype PIN, 5340/1232, wetted with 96% ethanol. B, Interpretative line drawing. Abbreviations: alc, alacrista; clp, clypeus; cs.b, costal bar; gul, gular plate; lb.p, labial palpus; lbr, labrum; lts, laterosternite; msi, median scutal impression; mta, metanepisternum; P1, supraantennal protuberance; pdl, pedicellus; scl2, mesoscutellum; s.lg, longitudinal suture; smt, submentum; s.stpl, sternopleural suture; tmp, temple; tr3, metatrochantin. Scale bars = 1 mm.
FIGURE 3. Jurodes ignoramus Ponomarenko, 1985 interpretative line drawings. A and B, Holotype. C and D, Paratype. E–G in Jurodidae (Coleoptera: Archostemata) from Transbaikalia: new findings and redescription of type material
FIGURE 3. Jurodes ignoramus Ponomarenko, 1985 interpretative line drawings. A and B, Holotype. C and D, Paratype. E–G, Original line drawings of the holotype from Ponomarenko, 1985 with minor changes. H, Details of holotype's head. I, Details of holotype's pronotum. K and J, Specimens from Khasurty locality. Abbreviations: alc, alacrista; an.cl, anapleural cleft; ant.g, antennal groove; ant.s, antennal socket; c.e, compound eye; clp, clypeus; cx3, metacoxae; em3, metepimeron; epl, epipleuron; eps2, mesanepisternum; es3, metanepisternum; fm1,2,3, pro-, meso-, metafemur; gen, genae; lbr, labrum; lts, laterosternite; md.p, pronotal median protuberance; P2, supraocular protuberance; P3, posteromesal protuberance; P4, posterolateral protuberance; po.e, postocular extension; ppl, propleuron; SIII, third abdominal sternite; sc2, mesoscutum; scl2, mesoscutellum; s.prc, paracoxal suture; TIX-X, abdominal tergites; tb1, protibia; tr1,2,3, pro- meso-, metatrochantin; trc1, protrochanter; v2, mesoventrite. All scale bars are equal to 1 mm.
FIGURE 5. Jurodes minor Ponomarenko, 1990 interpretative line drawings. A and B, Holotype. C and D in Jurodidae (Coleoptera: Archostemata) from Transbaikalia: new findings and redescription of type material
FIGURE 5. Jurodes minor Ponomarenko, 1990 interpretative line drawings. A and B, Holotype. C and D, Original line drawings of the holotype from Ponomarenko, 1990 with minor changes. E, Details of paratype's PIN, 3063/115 head. F–H, Paratypes PIN, 3063/115, 3063/1770 parts and counterparts, hindwings. I, Details of paratype's PIN, 3015/372 metathorax and abdomen. J, Paratype PIN, 3063/115. K, Paratype PIN, 3063/1262, metaventrite. L, Paratype PIN, 3015/365. Abbreviations: 11, apical antennomere; AA, anal vein; aed, aedeagus; alc, alacrista; an.cl, anapleural cleft; ant, antennae; ant.g, antennal groove; apm, apical membrane; C+ScA, costa fused with subcosta anterior; clp, clypeus; CuA, cubitus anterior; CuA2, cubitus anterior, second branch; cx3, metacoxae; em3, metepimeron; es3, metanepisternum; lbr, labrum; md.p, median protuberance; mpn3, metapostnotum; msi, median scutal impression; o, oblongum cell; P3, posteromesal protuberance; P4, posterolateral protuberance; po.e, postocular extension; RA, radius anterior; rc, radial cell; sc2, 3, meso- and metascutum; scl2, mesoscutellum; ScP, subcostal posterior; s.prc, paracoxal sutures; s.scl3, metathoracic scutoscutellar suture; TI-VIII, abdominal tergites; tb2, mesotibia; tr3, metatrochantin; trh3, metatrochanter. Figures G and H are given with the single scale bar. Scale bars = 1 mm.
FIGURE 4. Jurodes minor Ponomarenko, 1990. A and B in Jurodidae (Coleoptera: Archostemata) from Transbaikalia: new findings and redescription of type material
FIGURE 4. Jurodes minor Ponomarenko, 1990. A and B, Holotype part and counterpart PIN, 3015/1254, wetted with 96% ethanol. C and J, Paratype PIN, 3063/115 head and antennae and full body, wetted with 96% ethanol. D, F, H, Paratypes PIN, 3063/115, 3063/1770 parts and counterparts, hindwings wetted with 96% ethanol. Е, Paratype PIN, 3015/372 metathorax and abdomen, wetted with 96% ethanol. G and I, Material from Khasurty locality 5026/956 part and counterpart. K, Paratype PIN, 3015/365. L, Paratype PIN, 3063/1262, metaventrite. А and H are mirrored. Scale bars = 1 mm.
FIGURE 1. Jurodes ignoramus Ponomarenko, 1985. A in Jurodidae (Coleoptera: Archostemata) from Transbaikalia: new findings and redescription of type material
FIGURE 1. Jurodes ignoramus Ponomarenko, 1985. A, Holotype PIN, 3000/908 wetted with 96% ethanol. B, Holotype, counterpart wetted with 96% ethanol. C and D, Paratype PIN, 3000/911 part and counterpart. Scale bars = 1 mm.
Table S2: In Anorexia as a new type of adverse reaction caused by the COVID-19 vaccination: a case study applying detailed personal care records
<p><strong>Table S2</strong> Representative continuous care and vital data since April 2019 admission to August 2021 exit by participant death, and May to June data interrupting 2 June of COVID-19 vaccine injection were described in detail. 5 pre-injection disorder datasets were also included.</p>
FIGURES 1–7. 1 in Studies on type material from Kützing's diatom collection VI:The identity of Diatoma liber Suhr (1831)
FIGURES 1–7. 1. Reproduction of Suhr's original figure for Diatoma liber (in Suhr 1834, 17 (1), tab. III, fig. 4; Suhr's illustrations have no scale, the reproduction here is approximately the same size as that in the original, see https://www.biodiversitylibrary.org/page/ 31440#page/, also not to scale). 2–6. Specimens of Diatoma liber from BM 19390 ('Kützing 823', "Ins Canar.", Canary Islands). 7. Reproduction of Kützing's figures for Biddulphia quinquelocularis (in Kützing 1844, p. 138, pl. 19, fig. I, 1, 2). Scale bars: ca. 20 μm.
FIGURES 20–21. 20 in Studies on type material from Kützing's diatom collection VI:The identity of Diatoma liber Suhr (1831)
FIGURES 20–21. 20. Fragments of 'Biddulphia dalmatica' (?) from mica 'Kützing 822', "Adriatic, Dalmatica, Croatia". 21. A specimen of 'Diatoma maculosa Suhr' from BM 17984 ('Kützing 760', "Süd Occidentalis, Binder"). Scale bars: ca. 20 μm.
FIGURES 13–19. 13–16 in Studies on type material from Kützing's diatom collection VI:The identity of Diatoma liber Suhr (1831)
FIGURES 13–19. 13–16. Specimens of Biddulphia quinquelocularis from BM 19393 ('Kützing 1180', "Iles Chausey, France [Lenormand]). 17–19. Specimens of Biddulphia quinquelocularis from BM 19388 ('Kützing 934', "Lessina, Nolte [Germany]"). Scale bars: ca. 20 μm.
FIGURES 25–26. 25 in Studies on type material from Kützing's diatom collection VI:The identity of Diatoma liber Suhr (1831)
FIGURES 25–26. 25. Packet 'Kützing 823' ("Ins Canar.", Canary Islands). 26. Packet of material from Bory's herbarium in PC of Diatoma liber (TA 58393).
FIGURES 22–24. 22 in Studies on type material from Kützing's diatom collection VI:The identity of Diatoma liber Suhr (1831)
FIGURES 22–24. 22. Reproduction of Kützing's drawing of Biddulphia trilocularis (Kützing 1844, p. 138, pl. 29, fig. 89), possibly a reproduction or re-drawing of Ehrenberg's Denticella biddulphia (compare with Figs 23 and 24). 23, 24. Reproduction of Ehrenberg's Denticella biddulphia (Ehrenberg 1843, Taf. II, vi, fig. 19, 'Cuba', Fig. 23 = published drawing, Fig. 24 = unpublished drawing; none of the original illustrations have scales, the reproductions here are approximately the same size as that in the original)
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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.