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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>
FIGURE 4. Ischnura praematura morphological details and comparison with I in Ischnura praematura sp. nov. (Odonata: Zygoptera: Coenagrionidae): a species from Yunnan (China) whose females mate in the teneral state
FIGURE 4. Ischnura praematura morphological details and comparison with I. aurora collected in China (c–d), I. rubilio collected in India (e–f), and I. asiatica collected in China (g–h). a: lateral view of the last abdominal segments of I. praematura (♂); b: posterior view of the anal appendages of I. praematura (♂); c: lateral view of the last abdominal segments of I. aurora (♂); d: posterior view of the anal appendages of I. aurora (♂); e: lateral view of the last abdominal segments of I. rubilio (♂); f: posterior view of the anal appendages of I. rubilio (♂); g: lateral view of the last abdominal segments of I. asiatica (♂); h: posterior view of the anal appendages of I. asiatica (♂); i: dorsal view of the last abdominal segments of I. praematura (♂); j: lateral view of the last abdominal segments of I. praematura (♀). dt, dorsal tubercle; ce, cerci; p, paraprocts.
◂Fig. 6 Scanning electronmicroscopy images of Ramisyllis kingghidorahi n. sp. A Anterior region up to first 17 segments, dorsal view. B Prostomium in detail, anterodorsal view (broken antennae on stub). C Prostomium and first segments in detail showing dorsal bands of cilia, dorsal view. D–F Pores on dorsal cirri. Scale bars: 1 mm A, 200 µm B, 300 µm C, 50 µm E, 30 µm D, F in Ramisyllis kingghidorahi n. sp., a new branching annelid from Japan
◂Fig. 6 Scanning electronmicroscopy images of Ramisyllis kingghidorahi n. sp. A Anterior region up to first 17 segments, dorsal view. B Prostomium in detail, anterodorsal view (broken antennae on stub). C Prostomium and first segments in detail showing dorsal bands of cilia, dorsal view. D–F Pores on dorsal cirri. Scale bars: 1 mm A, 200 µm B, 300 µm C, 50 µm E, 30 µm D, F
◂Fig. 10 Scanning electron microscopy images of Ramisyllis kingghidorahi n. sp., posterior-most regions and epithelium details. A–D Posterior ends. Arrow in C and D points to heavily ciliated anus. E– G Minute crests on the dorsal surface of midbody segments. Arrows point to crests laterally located on the dorsal surface. H Dorsal surface of posterior segments. I Clumps of cilia on dorsal surface of proventricular segments. Arrows pointing to pores in H. Scale bars: 100 µm A, B, I, 50 um C, G, 5 µm D, E,4 µm F, and 3 µm H in Ramisyllis kingghidorahi n. sp., a new branching annelid from Japan
◂Fig. 10 Scanning electron microscopy images of Ramisyllis kingghidorahi n. sp., posterior-most regions and epithelium details. A–D Posterior ends. Arrow in C and D points to heavily ciliated anus. E– G Minute crests on the dorsal surface of midbody segments. Arrows point to crests laterally located on the dorsal surface. H Dorsal surface of posterior segments. I Clumps of cilia on dorsal surface of proventricular segments. Arrows pointing to pores in H. Scale bars: 100 µm A, B, I, 50 um C, G, 5 µm D, E,4 µm F, and 3 µm H
◂Fig. 9 Scanning electron microscopy images of branches of Ramisyllis kingghidorahi n. sp. A–F Midbody branching regions with segments of different morphologies, as long as wide with long dorsal cirri in A–C, much longer with short dorsal cirri in D, E and F Details of cirri alternation in length. A, C, E–F In dorsal view; B and D in ventral view. Scale bars: 200 µm A, C, 100 µm B, F, 400 µm D, and 500 µm E in Ramisyllis kingghidorahi n. sp., a new branching annelid from Japan
◂Fig. 9 Scanning electron microscopy images of branches of Ramisyllis kingghidorahi n. sp. A–F Midbody branching regions with segments of different morphologies, as long as wide with long dorsal cirri in A–C, much longer with short dorsal cirri in D, E and F Details of cirri alternation in length. A, C, E–F In dorsal view; B and D in ventral view. Scale bars: 200 µm A, C, 100 µm B, F, 400 µm D, and 500 µm E
Figs 19 & 20 in Detailed iconography of the widespread Neotropical millipede, Myrmecodesmus hastatus (Schubart, 1945), and the first record of the species from the Caribbean area (Diplopoda, Polydesmida, Pyrgodesmidae)
Figs 19 & 20. Right gonopod of a male of Myrmecodesmus hastatus (Schubart, 1945), from Saint-Pierre, Martinique, subventral and subdorsal views, respectively. Scale bar: 0.2 mm. Del. S. Golovatch. Designations: fl – flagellum; sl – solenomere.
Fig. 18 in Detailed iconography of the widespread Neotropical millipede, Myrmecodesmus hastatus (Schubart, 1945), and the first record of the species from the Caribbean area (Diplopoda, Polydesmida, Pyrgodesmidae)
Fig. 18. Habitus of a male of Myrmecodesmus hastatus (Schubart, 1945), from Saint-Pierre, Martinique, lateral view. Picture by D. VandenSpiegel.
FIGURE. Floral habit and structure of C. spongifolia. A. Type specimen in situ with open, spathe limb (apex is reflexed out of view), and green spathe tube (ca. 6 cm long). B. Adjacent plant with inflorescences and prophylls. C. Spadix showing from top: sterile appendix, staminate (male) zone, sterile interstice, and green pistillate (female) zone with tapered, conical form. D. Detail of female zone showing a few basal staminodes. E–G. Berries of the preserved type specimen. G. Dissected berry with orthotropous ovules (some outlined) attached by funicles to parietal placentae (arrows). H. Surface of male zone showing closely-packed synandria. I. Synandria separated to show fused anther sacs beneath apical pores (example in center has 8 pores, 8 anthers) J. Mature fruiting head, with single berry removed to show seed packing and 67 seeds extracted (scale bar units: 1 mm) (Bach Ma NP; type 2020; fruit and seeds 2018). Photos: NVD and PJM. in Colocasia spongifolia sp. nov. (Araceae) in southern China and central Vietnam
FIGURE. Floral habit and structure of C. spongifolia. A. Type specimen in situ with open, spathe limb (apex is reflexed out of view), and green spathe tube (ca. 6 cm long). B. Adjacent plant with inflorescences and prophylls. C. Spadix showing from top: sterile appendix, staminate (male) zone, sterile interstice, and green pistillate (female) zone with tapered, conical form. D. Detail of female zone showing a few basal staminodes. E–G. Berries of the preserved type specimen. G. Dissected berry with orthotropous ovules (some outlined) attached by funicles to parietal placentae (arrows). H. Surface of male zone showing closely-packed synandria. I. Synandria separated to show fused anther sacs beneath apical pores (example in center has 8 pores, 8 anthers) J. Mature fruiting head, with single berry removed to show seed packing and 67 seeds extracted (scale bar units: 1 mm) (Bach Ma NP; type 2020; fruit and seeds 2018). Photos: NVD and PJM.
Distribution. Lowland forests of W Brazil, E Peru, and N Bolivia, S of the Amazon River. Because of abundance of individuals in the C. castanea complex, hampering precise species identification in the field and in collections, a detailed assessment ofits distribution is still needed. in Phyllostomidae
Distribution. Lowland forests of W Brazil, E Peru, and N Bolivia, S of the Amazon River. Because of abundance of individuals in the C. castanea complex, hampering precise species identification in the field and in collections, a detailed assessment ofits distribution is still needed.
FIGURE 5. Legs details. A–B in Revealing the diversity of ant-eating spiders in Colombia I: morphology, distribution and taxonomy of the barronus group of the genus Tenedos O. Pickard-Cambridge, 1897 (Araneae: Zodariidae)
FIGURE 5. Legs details. A–B. Male of Tenedos barronus (MPUJ_ENT 0062009), leg IV: A. Tarsus, dorsal view. B. Same, retroventral view. C–D. Male of Tenedos andes Jocqué Baert, 2002 (ICN-Ar-8020), leg III: C. Tarsus, dorsal view (showing the trichobothriae row). D. Trichobothria. E–F. Male of Tenedos hoeferi Jocqué & Baert, 2002 (IBSP), leg III: E. Tarsus, ventral view. F. Idem, detail showing putative chemosensory setae.
FIGURE 4. Legs IV details. A–D in Revealing the diversity of ant-eating spiders in Colombia I: morphology, distribution and taxonomy of the barronus group of the genus Tenedos O. Pickard-Cambridge, 1897 (Araneae: Zodariidae)
FIGURE 4. Legs IV details. A–D. Male of Tenedos hoeferi (IBSP): A. Patella, retroventral view. B. Lyriform organ. C. Tibiametatarsus, dorsal view (arrow indicates the ball-shaped projection, an unambiguous synapomorphy of Zodariidae). D. Metatarsus-tarsus, dorsal view (arrow indicates vibration sense organ on metatarsus). E. Tarsus I, trichobothria. F. Tarsus I, tarsal organ. Abbreviations: MtS, metatarsal stopper.
FIGURE 2. Legs details. A–D in Revealing the diversity of ant-eating spiders in Colombia I: morphology, distribution and taxonomy of the barronus group of the genus Tenedos O. Pickard-Cambridge, 1897 (Araneae: Zodariidae)
FIGURE 2. Legs details. A–D. Male of Tenedos hoeferi (IBSP 276631), leg III: A. Metatarsus-tarsus, ventral view showing the chisel setae. B. Metatarsus distal side, ventral view. C–F. Male of Tenedos henrardi sp. n. (ICN-Ar-12341), leg II: C. Metatarsus, proventral view (arrow indicates the metatarsal stopper). D. Idem, ventral view (showing the chisel setae). E. Ventral view (showing the chisel setae). F. Chisel setae.
Calculating bond dissociation energies of X-H (X = C, N, O, S) bonds of aromatic systems via DFT: A detailed comparison of methods
<p>In this study, the bond dissociation energy (BDE) values of X-H (X = C, N, O, S) bonds of aromatic compounds were computed by using 17 different DFT functionals, namely M08-HX, M06-2X, M05-2X, M06, M05, BMK, MPW1B95, B1B95, B98, B97-2, LC-wPBE, B3LYP, cam-B3LYP, B2PLYP, MPWB1K, BB1K, BB95, within the basis set range 6-31G(d), 6-31+G(d), 6-31+G(d,p), 6-311G(d,p) and 6-311++G(d,p). The results show that the 6-31G(d) is the most convenient basis set to perform the BDE calculations with sufficient accuracy compared to the relevant experimental BDEs. The M06-2X, M05-2X, and M08-HX functionals gave highly accurate BDE values (with the average mean unsigned error MUE = 1.2-1.5 kcal/mol), performing better than the other functionals. The results suggest that the M06-2X, M05-2X, and M08-HX density functionals in the combined DFT/6-311+G(3df,2p)//B3LYP/6-31G(d) model chemistry offer the best method for calculating BDEs of ArX-H (X = C, N, O, S) bonds.</p>
Figs 1–17 in Detailed iconography of the widespread Neotropical millipede, Myrmecodesmus hastatus (Schubart, 1945), and the first record of the species from the Caribbean area (Diplopoda, Polydesmida, Pyrgodesmidae)
Figs 1–17. SEM micrographs of a male of Myrmecodesmus hastatus (SCHUBART, 1945), from Saint-Pierre, Martinique: habitus, lateral view (1); anterior part of body, lateral and dorsal views, respectively (2 & 5); midbody segments, lateral view (3); caudal part of body, lateral, dorsal and ventral views, respectively (4, 6 & 7); metatergal microsculpture, caudal view (8); cross-section of a midbody segment, caudal view (9); midbody paratergite, lateral view (10); tergal microsculpture with limbus, dorsal view (11); midbody sternite, ventral view (12); midbody leg, lateral view (13); left gonopod, submesal, subventral, subcaudal and mesal views, respectively (14–17). Scale bars: 0.5 mm (1), 0.1 mm (2–7 & 9), 0.05 mm (10 & 13–13), 0.02 mm (8, 11 & 12).
Plate I in First description of the male of Anagyrus almoriensis Shafee, Alam & Agarwal (Hymenoptera: Encyrtidae) with details of new host Pseudococcus calceolariae (Maskell) (Hemiptera: Pseudococcidae) on Rubus ellipticus (Rosaceae) from Himalayas
Plate I: Anagyrus almoriensis Shafee, Alam & Agarwal. Female on card (NIM (ICAR- NBAIR)) figures (1−3) 1. Female in habitus; 2. Antenna; 3. Fore wing.
Plate II in First description of the male of Anagyrus almoriensis Shafee, Alam & Agarwal (Hymenoptera: Encyrtidae) with details of new host Pseudococcus calceolariae (Maskell) (Hemiptera: Pseudococcidae) on Rubus ellipticus (Rosaceae) from Himalayas
Plate II. Anagyrus almoriensis Shafee, Alam & Agarwal. Female on slide (ZDAMU) figures (4−9) 4. Head, 5. Head showing raised reticulate sculpture; 6. Mesoscutum setae; 7. Scutellum setae; 8 & 9. Ovipositor
Plate III. Anagyrus almoriensis Shafee, Alam & Agarwal. Male on card (ZDAMU) figures (10−15) 10. Mandible; 11. Antenna; 12. Scape and pedicel sculpture; 13. Fore wing; 14. Metasoma; 15. Axillae and scutellum in First description of the male of Anagyrus almoriensis Shafee, Alam & Agarwal (Hymenoptera: Encyrtidae) with details of new host Pseudococcus calceolariae (Maskell) (Hemiptera: Pseudococcidae) on Rubus ellipticus (Rosaceae) from Himalayas
Plate III. Anagyrus almoriensis Shafee, Alam & Agarwal. Male on card (ZDAMU) figures (10−15) 10. Mandible; 11. Antenna; 12. Scape and pedicel sculpture; 13. Fore wing; 14. Metasoma; 15. Axillae and scutellum
FIGURE. Drosera tomentosa (a–d): a, rosette; b, rosette and base of inflorescences of D. tomentosa var. glabrata (Serra do Cipó, MG); c, inflorescence of the "type morphotype" of D. tomentosa (Chapada Diamantina, BA); d, inflorescence with open flower of the "glabrate morphotype" of D. tomentosa, side view (Diamantina, MG). Drosera villosa (e, f): e, habit; f, flower (Parque Estadual da Serra Negra da Mantiqueira, MG). Drosera viridis (g–i): g, rosettes of D. viridis (bottom) and D. communis (single plant, top; Imbituva, PR); h, leaf, detail (Piraquara, PR); i, flower (Balsa Nova, PR). Photo credits: a, b, d–f by PMG; c by FR; g–i by Carlos Rohrbacher. in A synopsis of the genus Drosera (Droseraceae) in Brazil
FIGURE. Drosera tomentosa (a–d): a, rosette; b, rosette and base of inflorescences of D. tomentosa var. glabrata (Serra do Cipó, MG); c, inflorescence of the "type morphotype" of D. tomentosa (Chapada Diamantina, BA); d, inflorescence with open flower of the "glabrate morphotype" of D. tomentosa, side view (Diamantina, MG). Drosera villosa (e, f): e, habit; f, flower (Parque Estadual da Serra Negra da Mantiqueira, MG). Drosera viridis (g–i): g, rosettes of D. viridis (bottom) and D. communis (single plant, top; Imbituva, PR); h, leaf, detail (Piraquara, PR); i, flower (Balsa Nova, PR). Photo credits: a, b, d–f by PMG; c by FR; g–i by Carlos Rohrbacher.
FIGURE. Drosera montana (a–c): a, rosette (Diamantina, MG); b, rosette (Parque Nacional do Itatiaia, RJ); c, rosettes with flowers (Parque Estadual da Serra de Ibitipoca, MG). Drosera quartzicola (d–f): d, habit with flower; e, habit; f, flower (Parque Nacional da Serra do Cipó, MG). Drosera riparia (g–i): g, habit of plant exposed to full sun; h, detail of leaves; i, inflorescence apex with open flower (Parque Nacional da Chapada Diamantina, BA). Photo credits: a, d, f by PMG; b by FR; c by Rodrigo Freitas; e by AF; g–i by Gabriel Garcia. in A synopsis of the genus Drosera (Droseraceae) in Brazil
FIGURE. Drosera montana (a–c): a, rosette (Diamantina, MG); b, rosette (Parque Nacional do Itatiaia, RJ); c, rosettes with flowers (Parque Estadual da Serra de Ibitipoca, MG). Drosera quartzicola (d–f): d, habit with flower; e, habit; f, flower (Parque Nacional da Serra do Cipó, MG). Drosera riparia (g–i): g, habit of plant exposed to full sun; h, detail of leaves; i, inflorescence apex with open flower (Parque Nacional da Chapada Diamantina, BA). Photo credits: a, d, f by PMG; b by FR; c by Rodrigo Freitas; e by AF; g–i by Gabriel Garcia.
FIGURE. Drosera hirtella: a, specimen Saint-Hilaire B1-1762bis (P00749158), with the designated lectotype highlighted; b, detail of the lectotype, showing the ascending scape and leaves with obovate lamina; c, detail of the individual to the left of the lectotype, representing the "western morphotype", with narrowly obovate lamina. Image extracted from A. de Saint-Hilaire virtual herbarium (2020). in A synopsis of the genus Drosera (Droseraceae) in Brazil
FIGURE. Drosera hirtella: a, specimen Saint-Hilaire B1-1762bis (P00749158), with the designated lectotype highlighted; b, detail of the lectotype, showing the ascending scape and leaves with obovate lamina; c, detail of the individual to the left of the lectotype, representing the "western morphotype", with narrowly obovate lamina. Image extracted from A. de Saint-Hilaire virtual herbarium (2020).
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.