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opencc-by-4.0Feb 2020View details →

Dataset for paper "Automatically Identifying Archival-worthy, Software-related Slack Conversations"

<p>This dataset consists of 2000 conversations from 5 programming related Q&A channels, hosted on Slack, and accompanies the paper "Automatically Identifying Archival-worthy, Software-related Slack Conversations". In addition to the text of the conversations, each conversation has been annotated as either archival worthy or not. Our definition of archival-worthiness is:</p> <p><em>"If a conversation contains information that could be useful to other users, whether in the Slack channel or elsewhere, then it should be archived. These conversations have no determinate length and no need for objectivity. A conversation should be archived based on the availability and ease of identifying information that could help a person to gain useful software-related knowledge."</em></p> <p><strong>Data Origin: </strong>Numerous public Slack chat channels (<a href="https://slack.com/">https://slack.com/</a>) have recently become available that are focused on specific software engineering-related discussion topics, e.g., Python Development (<a href="https://pyslackers.com/web/slack">https://pyslackers.com/web/slack</a>). The data reflects a portion of the conversations on public channels related to Python, Clojure, Elm and Racket programming.</p> <p><strong>Data Pre-Processing:</strong> To protect privacy, we replace usernames with fake names, and replace absolute times with relative times (in seconds). The conversations are disentangled from the overall chat stream with each unique <em>thread </em>in the dataset specifying a conversation in the channel. Archival-worthy conversations are marked with 1, while non-archival-worthy with 0.</p>

opencc-zeroMar 2020View details →

VAMDC extraction with identifier = 7974a04d-3adc-4d26-a1df-10c0e3be44ba

<div>This is a dataset extracted from http://vald.astro.uu.se/atoms-12.07/tap/ VAMDC node.</div><div>Query originating this dataset: query=select * where ( atomsymbol in ['h'] and radtranswavelength <= 11634.49275862069 and radtranswavelength >= 8827.596206896555 ); </div><div> Data source version: 2020-01-24</div><div>Data format: XSAMS 12.07</div><div>Query uuid in VAMDC query store: 7974a04d-3adc-4d26-a1df-10c0e3be44ba</div>

opencc-zeroMar 2020View details →

VAMDC extraction with identifier = 9202de74-a9b0-4e4d-9c1c-15a9673360bb

<div>This is a dataset extracted from http://topbase.obspm.fr/12.07/vamdc/tap/ VAMDC node.</div><div>Query originating this dataset: query=select * where ( atomsymbol in ['h'] and radtranswavelength <= 12450.010000000002 and radtranswavelength >= 2550.0100000000007 ); </div><div> Data source version: 2017-01-30</div><div>Data format: XSAMS 12.07</div><div>Query uuid in VAMDC query store: 9202de74-a9b0-4e4d-9c1c-15a9673360bb</div>

opencc-zeroJan 2020View details →

VAMDC extraction with identifier = 47ac70f9-ac49-410f-a8bd-801cf43cdf18

<div>This is a dataset extracted from https://cdms.astro.uni-koeln.de/cdms/tap/ VAMDC node.</div><div>Query originating this dataset: query=select * where ( inchikey in ['ugfairiumavxcw-uhfffaoysa-n'] and radtranswavelength <= 2.6075892488699395E7 and radtranswavelength >= 2.594919405550487E7 ); </div><div> Data source version: 2019-11-27</div><div>Data format: XSAMS 12.07</div><div>Query uuid in VAMDC query store: 47ac70f9-ac49-410f-a8bd-801cf43cdf18</div>

Fig. 19 in Integrative taxonomy identifies two new tardigrade species (Eutardigrada: Macrobiotidae) from Greenland

Fig. 19. Tenuibiotus zandrae sp. nov. Egg chorion morphology seen in SEM. A. Entire egg. B. Magnification of the egg surface. C–F. Details of the egg processes and surface between them. Filled flat arrowheads indicate thickenings/striae on the surface between processes and filled indented arrowheads indicate small tubercles on the process walls. Scale bars in μm.

Fig. 18 in Integrative taxonomy identifies two new tardigrade species (Eutardigrada: Macrobiotidae) from Greenland

Fig. 18. Tenuibiotus zandrae sp. nov. Egg chorion morphology seen in PCM. A. Midsection under 400× magnification. B. Surface under 400× magnification. C–D. Surface between processes under 1000× magnification. E–H. Midsections of processes of four different eggs under 1000× magnification. Filled flat arrowheads indicate thickenings/striae which are visible as dark dots and lines on the surface between processes. Scale bars in μm.

Fig. 14 in Integrative taxonomy identifies two new tardigrade species (Eutardigrada: Macrobiotidae) from Greenland

Fig. 14. Tenuibiotus zandrae sp. nov. Claws (paratypes). A–B. Claws II and IV seen in PCM, respectively. C–D. Claws I and IV seen in SEM, respectively. Filled indented arrowhead indicates horseshoe structure connecting the anterior and the posterior claw. Scale bars in μm.

Fig. 11 in Integrative taxonomy identifies two new tardigrade species (Eutardigrada: Macrobiotidae) from Greenland

Fig. 11. Tenuibiotus zandrae sp. nov. Body granulation seen in PCM (paratypes). A–B. Uniformly distributed granulation on the dorso-cephalic and dorso-caudal part of the body. C–D. Uniformly distributed granulation on the dorso-cephalic and dorso-caudal part of the body with small, random patches of lacking granulation. E–F. Uniformly distributed granulation on the ventral side of the body without and with small random patches lacking granulation, respectively. A–B, E and C–D, F are from two different paratypes. Scale bars in μm.

Fig. 8 in Integrative taxonomy identifies two new tardigrade species (Eutardigrada: Macrobiotidae) from Greenland

Fig. 8. Macrobiotus engbergi sp. nov. Egg chorion morphology seen in SEM. A. Entire egg. B. Magnification of the egg surface. C–D. Details of the terminal discs. Scale bars in μm.

Fig. 4 in Integrative taxonomy identifies two new tardigrade species (Eutardigrada: Macrobiotidae) from Greenland

Fig. 4. Macrobiotus engbergi sp. nov. Claws (paratypes). A–B. Claws III and IV seen in PCM, respectively. C–D. Claws III and IV seen in SEM, respectively. Filled flat arrowheads indicate double muscles attachments under the claws, empty flat arrowhead indicates inverted horseshoe structure under the external and the internal claw, whereas filled indented arrowhead indicates horseshoe structure connecting the anterior and the posterior claw. Scale bars in μm.

Fig. 5 in Integrative taxonomy identifies two new tardigrade species (Eutardigrada: Macrobiotidae) from Greenland

Fig. 5. Macrobiotus engbergi sp. nov. Buccal apparatus and the oral cavity armature seen in PCM (holotype, IZiBB, slide GL.052.22). A. Dorso-ventral projection of the entire buccal apparatus. B–C. Oral cavity armature visible in dorsal (B) and ventral (C) view, respectively. D–E. Placoid morphology visible in dorsal (D) and ventral (E) view, respectively. Filled flat arrowheads indicate the second band of teeth in the oral cavity, empty flat arrowheads indicate the third band of teeth in the oral cavity, empty indented arrowheads indicate central constrictions in the first macroplacoids and subterminal constriction in the second macroplacoids. Scale bars in μm.

Fig. 12 in Integrative taxonomy identifies two new tardigrade species (Eutardigrada: Macrobiotidae) from Greenland

Fig. 12. Tenuibiotus zandrae sp. nov. Patches of dense granulation on legs seen in PCM (paratypes). A. External granulation on leg III (patch of dense granulation encircled). B. Internal granulation on leg III. C. Granulation on leg IV. Scale bars in μm.

Fig. 21 in Integrative taxonomy identifies two new tardigrade species (Eutardigrada: Macrobiotidae) from Greenland

Fig. 21. Tenuibiotus voronkovi (Tumanov, 2007) Egg chorion morphology seen in PCM. A. Midsection under 400× magnification. B. Surface between processes under 1000× magnification. C–J. Details of egg processes under 1000× magnification. Filled flat arrowhead indicates thickenings/striae/sculpture which are visible as dark dots on the surface between processes and indented empty arrowheads indicate broken apices of the egg processes. Scale bars in μm.

Fig. 20 in Integrative taxonomy identifies two new tardigrade species (Eutardigrada: Macrobiotidae) from Greenland

Fig. 20. Tenuibiotus voronkovi (Tumanov, 2007). Body granulation seen in PCM. A. Uniformly distributed granulation of uniform size on the dorso-medial part of the body (cephalic region, paratype). B. Patch of dorso-lateral granulation composed of granules of different size (holotype). Scale bars in μm.

opencc-zeroApr 2020View details →

Natural history specimens collected and/or identified and deposited.

Natural history specimen data collected and/or identified by Copas, Kyle, <a href="https://orcid.org/0000-0002-6590-599X">https://orcid.org/0000-0002-6590-599X</a>. Claims were made on Bloodhound, <a href="http://bloodhound-tracker.net">https://bloodhound-tracker.net</a> using specimen data from the Global Biodiversity Information Facility, <a href="https://gbif.org">https://gbif.org</a>.

Figure 2 in Prospects for using DNA barcoding to identify spiders in species-rich genera

Figure 2. Box-and-whisker plots of average intraspecific divergence for 16 genera represented by more than 3 species (Neriene, Pimoa, and Theridion were excluded). The life history of each genus is also indicated.

Figure 1 in Prospects for using DNA barcoding to identify spiders in species-rich genera

Figure 1. Cumulative number of spider species described over time, including only species that are currently valid (description years for all valid species follow Platnick 2009).

Figure 5 in Prospects for using DNA barcoding to identify spiders in species-rich genera

Figure 5. Maximum intraspecific divergence compared with nearest-neighbor distance using all data for the four categories of topology: A monophyletic (133 cases), B nested (23 cases), C paraphyletic (28 cases), and D intermingled (16 case). See Methods for definitions. 89.7% of monophyletic and nested species fall above the 1:1 line, indicating the presence of a barcode gap, while 90.9% of paraphyletic and intermingled species fall below this line.

Figure 4 in Prospects for using DNA barcoding to identify spiders in species-rich genera

Figure 4. Maximum intraspecific divergence compared with nearest-neighbour distance of monophyletic morphospecies for all data and using only new data, which have been identified by a single spider taxonomist. Most species (92.5%) fall above the 1:1 line, indicating the presence of a "barcode gap".