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FIGURE 1 in Systematics of the endangered toad genus Andinophryne (Anura: Bufonidae): phylogenetic position and synonymy under the genus Rhaebo
FIGURE 1. (Continued)
FIGURE 2 in Systematics of the endangered toad genus Andinophryne (Anura: Bufonidae): phylogenetic position and synonymy under the genus Rhaebo
FIGURE 2. (Continued)
Semisitting Position and Venous Air Embolism in Neurosurgical Patients with Patent Foramen Ovale: A Systematic Analysis
<p>The semisitting position (SSP) offers significant advantages for neurosurgeons but presents numerous challenges to anesthesiologists. One major concern is venous air embolism (VAE). The incidence of patent foramen ovale (PFO) is approximately 10-35%. Typically, PFO causes a left-to-right shunt, but there is also a possibility of paradoxical embolism. Patients who undergo sitting craniotomies are routinely evaluated using a preoperative transthoracic echocardiogram (TTE) or transesophageal echocardiogram (TEE). Even in the presence of a PFO, neurosurgeons frequently prefer to perform surgery in the SSP. The incidence of venous air embolism in the sitting position is 23-45%. However, the rate of clinically significant air embolism is significantly lower. We conducted herein a systematic review of the incidence rates of PFO, venous air embolism, and complications in patients undergoing semisitting neurosurgical procedures. According to our analysis, the incidence of VAE was similar in both unknown and known PFO status patients (23.5% vs. 24.5%; p = 0.88) undergoing semisitting neurosurgical procedures. Other complications, such as hypotension, MI, stroke and perioperative deaths, could not be compared between the two groups due to inadequate power. However, there is a lack of level A evidence from currently available observational studies. Definitive evidence-based recommendations and guidelines based on well-designed studies are required to address this problem</p>
FIGURE 2 in Systematic position of Dinidoridae within the superfamily Pentatomoidea (Hemiptera: Heteroptera) revealed by the Bayesian phylogenetic analysis of the mitochondrial 12S and 16S rDNA sequences
FIGURE 2. Phylogenetic tree obtained from the Bayesian inference analysis of the 16S rDNA dataset.
FIGURE 1 in Systematic position of Dinidoridae within the superfamily Pentatomoidea (Hemiptera: Heteroptera) revealed by the Bayesian phylogenetic analysis of the mitochondrial 12S and 16S rDNA sequences
FIGURE 1. Phylogenetic tree obtained from the Bayesian inference analysis of the 12S rDNA dataset.
Supplementary material 2 from: Chen H-P, Kikuchi N, Shiao S-F (2024) Discovery of a new Pseudalomya Telenga, 1930 (Hymenoptera, Ichneumonidae, Ichneumoninae) species from Taiwan and its implications for the systematic position of this genus. Journal of Hymenoptera Research 97: 277-296. https://doi.org/10.3897/jhr.97.119470
PCR primers and conditions used in this study
Supplementary material 3 from: Chen H-P, Kikuchi N, Shiao S-F (2024) Discovery of a new Pseudalomya Telenga, 1930 (Hymenoptera, Ichneumonidae, Ichneumoninae) species from Taiwan and its implications for the systematic position of this genus. Journal of Hymenoptera Research 97: 277-296. https://doi.org/10.3897/jhr.97.119470
Fasta and Nexus files for the analysis in this study
Supplementary material 1 from: Chen H-P, Kikuchi N, Shiao S-F (2024) Discovery of a new Pseudalomya Telenga, 1930 (Hymenoptera, Ichneumonidae, Ichneumoninae) species from Taiwan and its implications for the systematic position of this genus. Journal of Hymenoptera Research 97: 277-296. https://doi.org/10.3897/jhr.97.119470
Sequences used in this study
Figure 7 from: Chen H-P, Kikuchi N, Shiao S-F (2024) Discovery of a new Pseudalomya Telenga, 1930 (Hymenoptera, Ichneumonidae, Ichneumoninae) species from Taiwan and its implications for the systematic position of this genus. Journal of Hymenoptera Research 97: 277-296. https://doi.org/10.3897/jhr.97.119470
Figure 7 Maximum likelihood phylogenetic trees of Ichneumoninae reconstructed using the COI and 28S datasets (COI: 648 bp; GTR+F+I+G4 [1–648\3 and 2–648\3 bp]; HKY+F+I+G4 [3–648\3 bp]; 28S: 625 bp; GTR+F+I+G4 [1–625 bp]). The red and blue colors indicate Phaeogenini and Alomyini, respectively. Branch lengths of the phylogenetic trees are proportional to the infer number of nucleotide substitutions per site, except for the branch of the outgroup Agriotypus armatus. Circles on the nodes indicate different SH-aLRT/UFBoot values. Nodal support with an SH-aLRT value of <80% and a UFBoot value of <95% is not shown. Abbreviations: SH-aLRT, SH-like approximate likelihood ratio test; UFBoot, ultrafast bootstrap approximation; XOR, one or the other but not both.
Figure 4 from: Chen H-P, Kikuchi N, Shiao S-F (2024) Discovery of a new Pseudalomya Telenga, 1930 (Hymenoptera, Ichneumonidae, Ichneumoninae) species from Taiwan and its implications for the systematic position of this genus. Journal of Hymenoptera Research 97: 277-296. https://doi.org/10.3897/jhr.97.119470
Figure 4 Characters of two Pseudalomya species. Frontal horns: APseudalomya truncaticornis sp. nov. (holotype, NMNS ENT 8836-1) BPseudalomya nepalensis (holotype, SDEI). Faces: CP. truncaticornis sp. nov. (holotype, NMNS ENT 8836-1) DP. nepalensis (holotype, SDEI) E darker specimen of P. truncaticornis sp. nov. (paratype, NMNS ENT 8836-2), dorsal view of the head F darker specimen of P. truncaticornis sp. nov. (paratype, NMNS ENT 8836-2), lateral view of the head. Illustrated and photographed by Hsuan-Pu Chen (A–C, E, F) and Matthias Riedel (D).
Figure 6 from: Chen H-P, Kikuchi N, Shiao S-F (2024) Discovery of a new Pseudalomya Telenga, 1930 (Hymenoptera, Ichneumonidae, Ichneumoninae) species from Taiwan and its implications for the systematic position of this genus. Journal of Hymenoptera Research 97: 277-296. https://doi.org/10.3897/jhr.97.119470
Figure 6 Maximum likelihood phylogenetic tree of Ichneumoninae reconstructed using the concatenated 18S+28S+COI dataset (2575 bp; 18S: 1302 bp; 28S: 625 bp; COI: 648 bp; SYM+I+G4 [1–1302, 1303–1927, 1928–2575\3, and 1929–2575\3 bp]; HKY+F+I+G4 [1930–2575\3 bp]). The red and blue colors indicate Phaeogenini and Alomyini, respectively. Branch lengths of the phylogenetic tree are proportional to the infer number of nucleotide substitutions per site, except for the branch of the outgroup Agriotypus armatus. Circles on the nodes indicate different SH-aLRT/UFBoot values. Nodal support with an SH-aLRT value of <80% and a UFBoot value of <95% is not shown. Abbreviations: SH-aLRT, SH-like approximate likelihood ratio test; UFBoot, ultrafast bootstrap approximation; XOR, one or the other but not both.
Figure 5 from: Chen H-P, Kikuchi N, Shiao S-F (2024) Discovery of a new Pseudalomya Telenga, 1930 (Hymenoptera, Ichneumonidae, Ichneumoninae) species from Taiwan and its implications for the systematic position of this genus. Journal of Hymenoptera Research 97: 277-296. https://doi.org/10.3897/jhr.97.119470
Figure 5 Habitat of Pseudalomya truncaticornis sp. nov. in Mount Huoshi (24°22'47.78"N, 121°10'53.67"E DMS), Shei-Pa National Park. Photographed by Ta-Hsiang Lee.
Figure 3 from: Chen H-P, Kikuchi N, Shiao S-F (2024) Discovery of a new Pseudalomya Telenga, 1930 (Hymenoptera, Ichneumonidae, Ichneumoninae) species from Taiwan and its implications for the systematic position of this genus. Journal of Hymenoptera Research 97: 277-296. https://doi.org/10.3897/jhr.97.119470
Figure 3 Pseudalomya truncaticornis sp. nov., NMNS ENT 8836-1 (A), NMNS ENT 8836-2 (B), and NARO (C) A lateral view of the mesosoma B wings C metasomal sternites. Photographed by Hsuan-Pu Chen (A, B) and Namiki Kikuchi (C).
Figure 1 from: Chen H-P, Kikuchi N, Shiao S-F (2024) Discovery of a new Pseudalomya Telenga, 1930 (Hymenoptera, Ichneumonidae, Ichneumoninae) species from Taiwan and its implications for the systematic position of this genus. Journal of Hymenoptera Research 97: 277-296. https://doi.org/10.3897/jhr.97.119470
Figure 1 Pseudalomya truncaticornis sp. nov. holotype (NMNS ENT 8836-1) A lateral view of the habitus B dorsal view of the habitus. Photographed by Hsuan-Pu Chen.
Figure 2 from: Chen H-P, Kikuchi N, Shiao S-F (2024) Discovery of a new Pseudalomya Telenga, 1930 (Hymenoptera, Ichneumonidae, Ichneumoninae) species from Taiwan and its implications for the systematic position of this genus. Journal of Hymenoptera Research 97: 277-296. https://doi.org/10.3897/jhr.97.119470
Figure 2 Pseudalomya truncaticornis sp. nov. holotype (NMNS ENT 8836-1) A dorsal view of the head B anterior view of the head C lateral view of the head D foreleg E dorsal view of the mesoscutum F dorsal view of the propodeum G dorsal view of the metasomal tergites. Photographed by Hsuan-Pu Chen.
Table 2 in Two new related oodine genera in the Oriental Region, with remarks on the systematic position of the genera Hololeius and Holosoma (Coleoptera, Carabidae)
<p>Table 2. Diagnostic character state combinations shown by exemplars of Hololeius ceylanicus and Hololeius cyaneus.</p><table><tbody><tr><th>No.</th><th>Characters</th><th>Hololeius ceylanicus</th><th>Hololeius cyaneus</th></tr></tbody><tbody><tr><td>01</td><td>Pubescence of integument</td><td>partly pubescent</td><td>glabrous</td></tr><tr><td>02</td><td>Punctuation of integument</td><td>punctate (Figs 1-3)</td><td>impunctate (Figs 13-16)</td></tr><tr><td>03</td><td>Antennomere 3</td><td>with a few short and scattered setae</td><td>glabrous</td></tr><tr><td>04</td><td>Mentum tooth form anteriorly</td><td>truncate</td><td>rounded</td></tr><tr><td>05</td><td>PW/PL</td><td>1.14-1.15 (Fig. 1)</td><td>1.24-1.37 (Fig. 13)</td></tr><tr><td>06</td><td>Basal margin of pronotum at posterior angles</td><td>oblique (Fig. 1)</td><td>gradually rounded (Fig. 13)</td></tr><tr><td>07</td><td>Pronotum</td><td>bordered laterally and lateroapically, not bordered medioapically and basally (Fig. 1)</td><td>bordered throughout (Fig. 13)</td></tr><tr><td>08</td><td>Elytral striae 1-8</td><td>1-7 punctate, 8 impunctate (Fig. 2)</td><td>impunctate (Fig. 14)</td></tr><tr><td>09</td><td>Stria 8</td><td>not or hardly deeper than other striae (Figs 2-3)</td><td>evidently deeper than other striae (Figs 14-16)</td></tr><tr><td>10</td><td>Elytral intervals</td><td>punctate (Figs 2-3)</td><td>impunctate (Figs 14-16)</td></tr><tr><td>11</td><td>Interval 9</td><td>distinct throughout</td><td>transformed into marginal gutter along anterior 2/5 of elytra, distinct in posterior 3/5</td></tr><tr><td>12</td><td>Number of umbilicate pores</td><td>23-25</td><td>15-16</td></tr><tr><td>13</td><td>Mesocoxa lateral margin</td><td>with one long seta</td><td>without seta</td></tr><tr><td>14</td><td>Joins of claws</td><td>opposite, distantly situated from each other</td><td>nearly parallel, closely situated to each other (Figs 14-15)</td></tr><tr><td>15</td><td>Number of pores on last sternum in female</td><td>four pores</td><td>two pores</td></tr><tr><td>16</td><td>Apical stylomere of ovipositor</td><td>subtriangular, as wide as basal stylomere, with 36 long ensiform setae at dorsomedial, dorsolateral and ventral position, and with nematiform setae, shorter than ensiform setae (Figs 10-11)</td><td>subelongate, nearly twice as narrow as basal stylomere, with 11 short ensiform setae at dorsomedial and dorsolateral position, and with nematiform setae, nearly twice as long as ensiform setae (Figs 17-18)</td></tr></tbody></table>
Table 1 in Two new related oodine genera in the Oriental Region, with remarks on the systematic position of the genera Hololeius and Holosoma (Coleoptera, Carabidae)
<p>Table 1. List of the Oriental genera of Oodini, their species number and distribution.</p><table><tbody><tr><th>Genera</th><th>Species</th><th>Distribution (incl. unpublished data)</th></tr></tbody><tbody><tr><td>Anatrichis LeConte, 1853</td><td>3</td><td>Indian subcontinent, Myanmar, Philippines</td></tr><tr><td>Bamaroodes B. Guéorguiev, gen. n.</td><td>1</td><td>Myanmar, Thailand</td></tr><tr><td>Brachyodes Jeannel, 1949</td><td>4</td><td>whole region</td></tr><tr><td>Holcocoleus Chaudoir in Oberthur, 1883</td><td>2</td><td>India (Tamil Nadu), Ceylon</td></tr><tr><td>" Holosoma boettcheri Jedlička, 1936 "</td><td>1</td><td>Philippines</td></tr><tr><td>Megaloodes Lesne, 1896</td><td>1</td><td>SE Thailand, E Cambodia</td></tr><tr><td>Miltodes Andrewes, 1922</td><td>1</td><td>India, Thailand, Sumatra</td></tr><tr><td>Nanodiodes Bousquet, 1996</td><td>3</td><td>Ceylon, SE Asia, Indonesia, Philippines</td></tr><tr><td>Oodes Bonelli, 1810</td><td>16</td><td>whole region</td></tr><tr><td>Oodinus Motschulsky, 1864</td><td>1</td><td>Vietnam, Sumatra, Moluccas, Philippines</td></tr><tr><td>Pseudosphaerodes Jeannel, 1949</td><td>2</td><td>Myanmar, Philippines</td></tr><tr><td>Simous Chaudoir, 1882</td><td>9</td><td>whole region east of Bengal</td></tr><tr><td>Systolocranius Chaudoir, 1857</td><td>1</td><td>“Bengal”: MNHUB; "Ind. or.": NMW</td></tr><tr><td>Thaioodes B. Guéorguiev, gen. n.</td><td>1</td><td>Thailand</td></tr></tbody></table>
Figure 4 from: Chen H-L, Al-Shehbaz IA, Qian L-S, Zhang J-W, Xu B, Zhang T-C, Yue J-P, Sun H (2022) Pulvinatusia (Brassicaceae), a new cushion genus from China and its systematic position. PhytoKeys 189: 9-28. https://doi.org/10.3897/phytokeys.189.77926
Figure 4 Maximum Likelihood cladogram of the Brassicaceae based on the plastome dataset. Maximum likelihood bootstraps (BS) are noted above the branch. Three Lineages of Brassicaceae (Beilstein et al. 2006; Walden et al. 2020) were marked.
Figure 3 from: Chen H-L, Al-Shehbaz IA, Qian L-S, Zhang J-W, Xu B, Zhang T-C, Yue J-P, Sun H (2022) Pulvinatusia (Brassicaceae), a new cushion genus from China and its systematic position. PhytoKeys 189: 9-28. https://doi.org/10.3897/phytokeys.189.77926
Figure 3 Bayesian Inference topology of the Brassicaceae relationships based on the nuclear ITS dataset. Bayesian inference posterior probability (PP) and maximum parsimony bootstrap (BS) are noted.
Figure 2 from: Chen H-L, Al-Shehbaz IA, Qian L-S, Zhang J-W, Xu B, Zhang T-C, Yue J-P, Sun H (2022) Pulvinatusia (Brassicaceae), a new cushion genus from China and its systematic position. PhytoKeys 189: 9-28. https://doi.org/10.3897/phytokeys.189.77926
Figure 2 Images of Pulvinatusia xuegulaensisA and B fruiting plants C fruits D septum and replum E and F seeds G and H flowering plants I and J stems K leaves. Scales bars: 1 mm. – Photos: A–F & I–K by Lishen Qian G and H by Jianwen Zhang.
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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)
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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.