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Figure 9 from: Chan BKK, Tsao YF, Ganmanee M (2020) Morphological and molecular evidence support the intertidal barnacle Octomeris intermedia Nilsson-Cantell, 1921 (Thoracica, Chthamalidae) as a valid species in Indo-Pacific waters. ZooKeys 914: 1-31. https://doi.org/10.3897/zookeys.914.49328

Figure 9 Octomeris brunnea. A Mandible. B First tooth of mandible. C Second and third teeth of mandible. D Lower margin. E Mandibular palp. F Serrulate setae at outer margin of mandibular palp. G Labrum. H Small teeth on middle part of cutting edge of labrum. Scale bars in μm.

Figure 8 from: Chan BKK, Tsao YF, Ganmanee M (2020) Morphological and molecular evidence support the intertidal barnacle Octomeris intermedia Nilsson-Cantell, 1921 (Thoracica, Chthamalidae) as a valid species in Indo-Pacific waters. ZooKeys 914: 1-31. https://doi.org/10.3897/zookeys.914.49328

Figure 8 Octomeris brunnea (CEL-KT-131, Hai Kou, Taiwan). A Maxilla. B Magnified view of distal lobe showing serrulate setae. C Inner margin of proximal lobe of maxilla showing serrulate setae. D Outer margin of maxilla showing serrulate setae. E Maxillule; note the two deep notches on upper and lower 1/3 of the cutting edge. F Cutting edge above upper notch. G Middle portion of cutting edge. H Lower portion of cutting edge below lower notch. Scale bars in μm.

Figure 6 from: Chan BKK, Tsao YF, Ganmanee M (2020) Morphological and molecular evidence support the intertidal barnacle Octomeris intermedia Nilsson-Cantell, 1921 (Thoracica, Chthamalidae) as a valid species in Indo-Pacific waters. ZooKeys 914: 1-31. https://doi.org/10.3897/zookeys.914.49328

Figure 6 Octomeris brunnea (CEL-KT-131, Hai Kou, Taiwan). A Cirrus III. B Intermediate segments of posterior ramus of cirrus III. C Distal segments of anterior ramus of cirrus III. D. Simple type setae on anterior ramus of cirrus III. E Cirrus IV. F Intermediate segments of cirrus IV. G Dorsal surface of proximal segment of posterior ramus of cirrus IV. H Distal segments of anterior ramus of cirrus IV. Scale bars in μm.

Figure 14 from: Chan BKK, Tsao YF, Ganmanee M (2020) Morphological and molecular evidence support the intertidal barnacle Octomeris intermedia Nilsson-Cantell, 1921 (Thoracica, Chthamalidae) as a valid species in Indo-Pacific waters. ZooKeys 914: 1-31. https://doi.org/10.3897/zookeys.914.49328

Figure 14 Octomeris intermedia (CEL-Thai-359, Krabi, Thailand). A Mandible, whole view B First and second teeth of mandible. C Second and third teeth of mandible of another specimen. D Lower margin of mandible. E Distal part of mandibular palp. F Serrulate setae at distal margin of mandibular palp. G Labrum. H Cutting edge of labrum, middle part. Scale bars in μm.

Figure 17 from: Chan BKK, Tsao YF, Ganmanee M (2020) Morphological and molecular evidence support the intertidal barnacle Octomeris intermedia Nilsson-Cantell, 1921 (Thoracica, Chthamalidae) as a valid species in Indo-Pacific waters. ZooKeys 914: 1-31. https://doi.org/10.3897/zookeys.914.49328

Figure 17 The neighbor-joining trees reconstructed with COI A and 12S rRNA B by MEGA X. Bootstrap values above 90 are represented at the nodes. "*" indicates the sequences from Fisher et al. (2004) and Pérez-Losada et al. (2012), which were designated as O. brunnea in their studies.

Figure 13 from: Chan BKK, Tsao YF, Ganmanee M (2020) Morphological and molecular evidence support the intertidal barnacle Octomeris intermedia Nilsson-Cantell, 1921 (Thoracica, Chthamalidae) as a valid species in Indo-Pacific waters. ZooKeys 914: 1-31. https://doi.org/10.3897/zookeys.914.49328

Figure 13 Octomeris intermedia (CEL-Thai-359, Krabi, Thailand). A Maxilla. B Magnified view of distal lobe showing serrulate setae. C Inner margin of maxilla showing serrulate setae. D Outer margin of maxilla showing serrulate setae. E Maxillule; note the two shallow notches on upper and lower 1/3 of the cutting edge. F Cutting edge above upper notch. G Middle portion of cutting edge. H Lower portion of cutting edge. Scale bars in μm.

Figure 5 from: Chan BKK, Tsao YF, Ganmanee M (2020) Morphological and molecular evidence support the intertidal barnacle Octomeris intermedia Nilsson-Cantell, 1921 (Thoracica, Chthamalidae) as a valid species in Indo-Pacific waters. ZooKeys 914: 1-31. https://doi.org/10.3897/zookeys.914.49328

Figure 5 Octomeris brunnea (CEL-KT-131, Hai Kou, Taiwan). A Cirrus I. B Posterior ramus of cirrus I. C Bidentate serrate setae at tip of segment. D Bidentate serrate setae at tip of anterior ramus. E Cirrus II. F Dorsal side of posterior ramus. G, H Bidentate serrate setae at posterior ramus. Scale bars in μm.

Figure 3 from: Chan BKK, Tsao YF, Ganmanee M (2020) Morphological and molecular evidence support the intertidal barnacle Octomeris intermedia Nilsson-Cantell, 1921 (Thoracica, Chthamalidae) as a valid species in Indo-Pacific waters. ZooKeys 914: 1-31. https://doi.org/10.3897/zookeys.914.49328

Figure 3 Shape of the tergo-scutal junction (TS junction, indicated by arrows) of Octomeris brunnea (CEL-KT-131, Hai Kou, Taiwan) and O. intermedia (CEL-Thai-359, Krabi, Thailand) All specimens share the same scale bar.

Figure 16 from: Chan BKK, Tsao YF, Ganmanee M (2020) Morphological and molecular evidence support the intertidal barnacle Octomeris intermedia Nilsson-Cantell, 1921 (Thoracica, Chthamalidae) as a valid species in Indo-Pacific waters. ZooKeys 914: 1-31. https://doi.org/10.3897/zookeys.914.49328

Figure 16 Consistent differences in the presences of shallow and deep notches on the cutting edge of O. intermedia (A-C) CEL-Thai-359, Krabi, Thailand) and O. brunnea (D-F) (CEL-KT-131, Hai Kou, Taiwan), respectively. The notches in O. brunnea are much deeper, and three distinct regions can be seen along the cutting edge. Scale bars in μm.

Figure 2 from: Chan BKK, Tsao YF, Ganmanee M (2020) Morphological and molecular evidence support the intertidal barnacle Octomeris intermedia Nilsson-Cantell, 1921 (Thoracica, Chthamalidae) as a valid species in Indo-Pacific waters. ZooKeys 914: 1-31. https://doi.org/10.3897/zookeys.914.49328

Figure 2 A Krabi, Thailand, showing O. intermedia at the overhang of an intertidal cave (indicated by white arrow). B Hey or Coral Island, Phuket, showing that O. intermedia occur on shaded rocks. CO. intermedia can occupy up to 100% cover under a shaded rock in Thailand. DOctomeris intermedia, showing partially eroded samples, with longitudinal furrows at the base of the shell plates. EO. intermedia, eroded samples, showing shell with a smooth surface. FO. intermedia, uneroded samples, showing longitudinal furrows on the surface. GO. brunnea on Lanyu, Taiwan. Shell is more conical than O. intermedia. Eroded sample with smooth shell plates.

opengpl-2.0-or-laterNov 2019View details →

TTnet - Model validation data

This repository contains the raw data collected to validate the TTnet time and energy model, which is described in <ul> <li>Time-Triggered Wireless Architecture Romain Jacob, Licong Zhang, Marco Zimmerling, Samarjit Chakraborty, Lothar Thiele    Accepted to ECRTS 2020   <a href="https://arxiv.org/abs/2002.07491">arxiv.org/abs/2002.07491</a></li> <li>Leveraging Synchronous Transmissions for the Design of Real-time Wireless Cyber-Physical Systems Romain Jacob Doctoral dissertation , 2020 <a href="https://doi.org/10.5281/zenodo.3510184">10.5281/zenodo.3510184 </a>(Chapter 5)</li> </ul> The processing of these data is described in detailed in the following GitHub repository: <a href="https://github.com/romain-jacob/TTW-Artifacts">github.com/romain-jacob/TTW-Artifacts</a> Files description <ul> <li>data_raw.zip Contains the serial logs and test configuration files, for all three test series</li> <li>serieX_all_data.zip Contains all the test results (serial logs + GPIO traces + power traces) for the test of series X. Missing for series 3 (we forgot to save it before it got deleted from the server... sorry about that)</li> </ul>

opennotspecifiedMar 2019View details →

FIGURE 30 in A review of the flying fish genus Cypselurus (Beloniformes: Exocoetidae). Part 1. Revision of the subgenus Zonocypselurus Parin and Bogorodsky, 2011 with descriptions of one new subgenus, four new species and two new subspecies and reinstatement of one species as valid

FIGURE 30. Exocoetus hexazona. After Bleeker (1866–1872; Plate SCOMBRES V, fig.3).

opennotspecifiedMar 2019View details →

FIGURE 23 in A review of the flying fish genus Cypselurus (Beloniformes: Exocoetidae). Part 1. Revision of the subgenus Zonocypselurus Parin and Bogorodsky, 2011 with descriptions of one new subgenus, four new species and two new subspecies and reinstatement of one species as valid

FIGURE 23. Holotype of flying fish Cypselurus bosha (147 mm SL, IORAS 03435, Bolinao fish market).

opencc-by-4.0Apr 2009View details →

Figure 2 in The Platycerus (Coleoptera, Lucanidae) of California, with the recognition of Platycerus cribripennis Van Dyke as a valid species

Figure 2. Male genitalia of P. cribripennis, with sclerotized flagellum on the everted internal sac.

Development and validation of a machine learning model for use as an automated artificial intelligence tool to predict mortality risk in patients with COVID-19

Background New York City quickly became an epicenter of the COVID-19 pandemic. Due to a sudden and massive increase in patients during COVID-19 pandemic, healthcare providers incurred an exponential increase in workload which created a strain on the staff and limited resources. As this is a new infection, predictors of morbidity and mortality are not well characterized. Methods We developed a prediction model to predict patients at risk for mortality using only laboratory, vital and demographic information readily available in the electronic health record on more than 3000 hospital admissions with COVID-19. A variable importance algorithm was used for interpretability and understanding of performance and predictors. Findings We built a model with 84-97% accuracy to identify predictors and patients with high risk of mortality, and developed an automated artificial intelligence (AI) notification tool that does not require manual calculation by the busy clinician. Oximetry, respirations, blood urea nitrogen, lymphocyte percent, calcium, troponin and neutrophil percentage were important features and key ranges were identified that contributed to a 50% increase in patients’ mortality prediction score. With an increasing negative predictive value (NPV) starting 0.90 after the second day of admission, we are able more confidently able identify likely survivors. This study serves as a use case of a model with visualizations to aide clinicians with a better understanding of the model and predictors of mortality. Additionally, an example of the operationalization of the model via an AI notification tool is illustrated.

Experimental and Simulation Results of "Hemodynamic study in 3D printed stenotic coronary artery models: experimental validation and transient simulation"

This repository contains the experimental and simulation results of the submitted article "Hemodynamic study in 3D printed stenotic coronary artery models: experimental validation and transient simulation" by Carvalho, V., Rodrigues, N., Ribeiro, R., Costa, P., Lima, R., Teixeira, S.

Fig. 6 in On the taxonomic validity of Indian ground spiders: II. Genera Drassyllus Chamberlin, 1922 and Nodocion Chamberlin, 1922 (Araneae: Gnaphosidae)

Fig. 6. Setaphis browni (Tucker, 1923), ♀, holotype of Liodrassus mandae Tikader & Gajbe, 1977 (NZC-ZSI-5018/18). A. Habitus, dorsal view. B. Eyes of the same, dorsal view. C. Epigyne, ventral view. D. Same, dorsal view. E. Label from type bottle. Scale bars: A = 1 mm; B–D = 0.2 mm.

Fig. 3 in On the taxonomic validity of Indian ground spiders: II. Genera Drassyllus Chamberlin, 1922 and Nodocion Chamberlin, 1922 (Araneae: Gnaphosidae)

Fig. 3. Cryptodrassus mahabalei (Tikader, 1982) comb. nov., ♀, holotype of Drassyllus mahabalei Tikader, 1982 (NZC-ZSI-5044/18). A. Habitus, dorsal view. B. Eyes of the same, dorsal view. C. Epigyne, ventral view. D. Same, dorsal view. E. Label from type bottle. Scale bars: A = 2 mm; B = 0.5 mm; C–D = 0.2 mm.

Fig. 5 in On the taxonomic validity of Indian ground spiders: II. Genera Drassyllus Chamberlin, 1922 and Nodocion Chamberlin, 1922 (Araneae: Gnaphosidae)

Fig. 5. "Setaphis" solanensis (Tikader & Gajbe, 1977) comb. nov., ♀, holotype of Nodocion solanensis Tikader & Gajbe, 1977 (NZC-ZSI-5002/18). A. Habitus, dorsal view. B. Eyes of the same, dorsal view. C. Epigyne, ventral view. D. Same, dorsal view. E. Label from type bottle. Scale bars: A = 2 mm; B = 0.2 mm; C–D = 0.5 mm.