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Fig. 2. A. D in Three new species of Dolichoiulus millipedes from the underground of Gran Canaria, with notes on the circumscription of the genus (Diplopoda, Julida, Julidae)

Fig. 2. A. D. typhlocanaria sp. nov., male from Cueva de la Luna, midbody rings. Scale 0.1 mm. B. D. oromii sp. nov., detail of posterior margin of midbody ring, showing diagnostic setae. Scale 0.05 mm.

Fig. 4. Posterior gonopods, mesal views. A. D in Three new species of Dolichoiulus millipedes from the underground of Gran Canaria, with notes on the circumscription of the genus (Diplopoda, Julida, Julidae)

Fig. 4. Posterior gonopods, mesal views. A. D. typhlocanaria sp. nov., specimen from Barranco Draguillo. B. D. typhlocanaria sp. nov., specimen from Cueva de la Luna. C. D. oromii sp. nov. ap: anterior process, pp: posterior process, mp: mesomerital process. Scales 0.1 mm.

Fig. 6 in Three new species of Eupetersia Blüthgen, 1928 (Hymenoptera, Halictidae) from the Oriental Region

Fig. 6. Eupetersia yanegai sp. nov. A. ♂, end of metasoma with pygidial plate. B. ♀, end of metasoma without pygidial plate.

Fig. 1 in Three new species of Dolichoiulus millipedes from the underground of Gran Canaria, with notes on the circumscription of the genus (Diplopoda, Julida, Julidae)

Fig. 1. Size diagram for Dolichoiulus typhlocanaria sp. nov. The diagram shows number of podous (leg-bearing) body rings (p.r., x axis) and vertical body diameter in mm (y axis). For a given number of podous rings D. typhlocanaria sp. nov. is thicker than the two other species (see Fig. 5), and females are thicker than males.

opencc-by-4.0May 2020View details →

Three-hourly gridded volcanic ash emissions for the Eyjafjallajökull 2010 eruption

Forward simulations of the Eyjafjälla 2010 eruption with unit emissions. These files are used to create an emission estimate of a volcanic eruption. Each file corresponds to an individual emission time point, and contains 19 individual emission simulations. Each emission simulation emits 1 teragram of ash into a unique vertical level of the model. The levels are labeled L01 .. L19, and designate level number from the top of the atmosphere (top of level 1 is close to 130 hPa or around 14 km ASL). The hybrid sigma levels are defined in Vertical_levels_22_650m.txt.  The files were created using eEMEP Unimod_ASH compiled by Alvaro Valdebenito (module  cams50/201809) on the Nebula supercomputer.

opencc-by-4.0Jul 2019View details →

Supplementary Data: A Frequentist Analysis of Three Right-Handed Neutrinos with GAMBIT

Supplementary Data  A Frequentist Analysis of 3 Right-Handed Neutrinos with GAMBIT. The files in this record contain data for the frequentist global fit of a model with three right-handed neutrinos using the <a href="http://gambit.hepforge.org">GAMBIT</a> tool.

Fig. 6 in Capalictus, a new subgenus of Lasioglossum Curtis, 1833 from South Africa, with description of three new species (Hymenoptera, Apoidea, Halictidae)

Fig. 6. Lasioglossum (Capalictus) tigrinum sp. nov., Ƌ. A. Head and forelegs. B. Mesoscutum and scutellum. C. Propodeum and metanotum. D. Metasoma, dorsal view. E. First tergum. F. Metasoma ventral view. Scale line = 0,5 mm.

Fig. 5 in Capalictus, a new subgenus of Lasioglossum Curtis, 1833 from South Africa, with description of three new species (Hymenoptera, Apoidea, Halictidae)

Fig. 5. Lasioglossum (Capalictus) hantamense sp. nov., ♀. A. Head. B. Mesoscutum and scutellum. C. Propodeum and metanotum. D. First tergum. E. Metasoma. Scale line = 0,5 mm.

Fig. 10. Dorsal habitus. — A-B in Capalictus, a new subgenus of Lasioglossum Curtis, 1833 from South Africa, with description of three new species (Hymenoptera, Apoidea, Halictidae)

Fig. 10. Dorsal habitus. — A-B. Lasioglossum mosselinum (Cockerell, 1945). A. ♀. B. Ƌ. — C-D. Lasioglossum timmermanni sp. nov. C. ♀. D. Ƌ. Scale line = 1 mm.

Fig. 18 in Capalictus, a new subgenus of Lasioglossum Curtis, 1833 from South Africa, with description of three new species (Hymenoptera, Apoidea, Halictidae)

Fig. 18. Summary of phylogenetic relationships of Capalictus relative to remaining Lasioglossum, based on Gibbs et al. 2012. Numbers represent posterior probability support values.

Fig. 1 in Capalictus, a new subgenus of Lasioglossum Curtis, 1833 from South Africa, with description of three new species (Hymenoptera, Apoidea, Halictidae)

Fig. 1. — Lasioglossum (Capalictus) mosselinum (Cockerell, 1945). A. Head showing lower paraocular area. C, E. Wing venation showing apex of marginal cell and weak veins of submarginal cells. C. ♀. E. Ƌ. F. ♀, propodeum and metapostnotum (dls = dorso- lateral slopes). — Lasioglossum (Afrodialictus) sp. B. Head showing lower paraocular area. — Lasioglossum (Sellalictus) sp. D. ♀, wing venation showing apex of marginal cell and weak veins of submarginal cells. Scale line = 0,5 mm.

Fig. 2 in Capalictus, a new subgenus of Lasioglossum Curtis, 1833 from South Africa, with description of three new species (Hymenoptera, Apoidea, Halictidae)

Fig. 2. Lasioglossum (Capalictus) mosselinum (Cockerell, 1945), ♀ holotype. A. Total view. B. Head. C. Mesosoma. D. Propodeum. E. First tergum. F. Metasoma. Scale line = 0,5 mm.

Fig. 16. A-D in Capalictus, a new subgenus of Lasioglossum Curtis, 1833 from South Africa, with description of three new species (Hymenoptera, Apoidea, Halictidae)

Fig. 16. A-D. Lateral view of mesosoma. E-F. Last terga. ♀♀. — A. Lasioglossum (Capalictus) mosselinum (Cockerell, 1945). — B. Lasioglossum (Capalictus) timmermanni sp. nov. — C. Lasioglossum (Capalictus) hantamense sp. nov. — D. Lasioglossum (Capalictus) tigrinum sp. nov. — E. Lasioglossum (Capalictus) mosselinum (Cockerell, 1945). — F. Lasioglossum (Capalictus) timmermanni sp. nov. Scale line = 0,5 mm.

opencc-by-4.0Mar 2020View details →

Consensus QSAR models estimating acute aquatic toxicity for three trophic levels organisms: Algae, Daphnia and Fish

We report new consensus models estimating acute toxicity for algae, daphnia and fish endpoints. We assembled a large collection of 3680 public unique compounds annotated by, at least, one experimental value for the given endpoint. Support Vector Machine models were internally and externally validated following the OECD principles. Reasonable predictive performances were achieved (RMSEext = 0.56 – 0.78) which are in line with those of state-of-the-art models. The known structural alerts are compared with analysis of the atomic contributions to these models obtained using the ISIDA/ColorAtom utility. A benchmarking against existing tools has been carried out on a set of compounds considered more representative and relevant for the chemical space of the current chemical industry. Our model scored one of the best accuracies and data coverage. Nevertheless, industrial data performances were noticeably lower than those on public data, indicating that existing models fail to meet the industrial needs. Thus, final models were updated with the inclusion of new industrial compounds, extending applicability domain and relevance for application in an industrial context. Generate models and collected public data are made freely available. Available fields in the SDF file: <ul> <li>SMILES_Canonical: canonical SMILES code</li> <li>DB: source of the data, "Litterature set" means that the data is originated from an article (see the companion article of the dataset for details).</li> <li>endpoint: organism for which endpoint is available</li> <li>CASRN: CAS registration number</li> <li>98-81-7</li> <li>pEC50 - DAPHNIA: Daphnia, mortality, which is evaluated by the immobilization of the invertebrate is recorded at 48 hours and expressed as the log median effective concentration (pEC50)</li> <li>mg/L - DAPHNIA: Daphnia, mortality, which is evaluated by the immobilization of the invertebrate is recorded at 48 hours and expressed as the median effective concentration (EC50)</li> <li>pLC50 - FISH: Fish, the log median lethal concentration measured at 96 hours is considered (pLC50)</li> <li>mg/L - FISH: Fish, the log median lethal concentration measured at 96 hours is considered (LC50)</li> <li>pEC50 - ALGA: Algae, the  purpose  is  to  determine  the substance’s growth inhibition effect, expressed as the log median effective concentration (pEC50) measured at 72 hours</li> <li>mg/L - ALGA: Algae, the  purpose  is  to  determine  the substance’s growth inhibition effect, expressed as the median effective concentration (EC50) measured at 72 hours</li> </ul>

Fig. 15 in Capalictus, a new subgenus of Lasioglossum Curtis, 1833 from South Africa, with description of three new species (Hymenoptera, Apoidea, Halictidae)

Fig. 15. Ƌ genitalia, dorsal view. — A. Lasioglossum (Capalictus) mosselinum (Cockerell, 1945). — B. Lasioglossum (Capalictus) timmermanni sp. nov. — C. Lasioglossum (Capalictus) hantamense sp. nov. — D. Lasioglossum (Capalictus) tigrinum sp. nov. Scale line = 0,25 mm.

Fig. 14 in Capalictus, a new subgenus of Lasioglossum Curtis, 1833 from South Africa, with description of three new species (Hymenoptera, Apoidea, Halictidae)

Fig. 14. Ƌ hind legs (left) and mid legs (right). — A-B. Lasioglossum (Capalictus) mosselinum (Cockerell, 1945). — C-D. Lasioglossum (Capalictus) timmermanni sp. nov. — E-F. Lasioglossum (Capalictus) hantamense sp. nov. — G-H. Lasioglossum (Capalictus) tigrinum sp. nov. Scale line = 0,5 mm.

Fig. 12 in Capalictus, a new subgenus of Lasioglossum Curtis, 1833 from South Africa, with description of three new species (Hymenoptera, Apoidea, Halictidae)

Fig. 12. Lateral habitus, Ƌ. — A. Lasioglossum (Capalictus) mosselinum (Cockerell, 1945). — B. Lasioglossum (Capalictus) timmermanni sp. nov. — C. Lasioglossum (Capalictus) hantamense sp. nov.. — D. Lasioglossum (Capalictus) tigrinum sp. nov. Scale line = 1 mm.

Fig. 11. Dorsal habitus. — A-B in Capalictus, a new subgenus of Lasioglossum Curtis, 1833 from South Africa, with description of three new species (Hymenoptera, Apoidea, Halictidae)

Fig. 11. Dorsal habitus. — A-B. Lasioglossum (Capalictus) hantamense sp. nov.. A. ♀. B. Ƌ. — C-D. Lasioglossum (Capalictus) tigrinum sp. nov. C. ♀. D. Ƌ. Scale line = 1 mm.

Fig. 4 in Capalictus, a new subgenus of Lasioglossum Curtis, 1833 from South Africa, with description of three new species (Hymenoptera, Apoidea, Halictidae)

Fig. 4. Lasioglossum (Capalictus) hantamense sp. nov., Ƌ. A. Head. B. Mesoscutum and scutellum. C. Propodeum and metanotum. D. First tergum. E. Metasoma, dorsal view. F. Metasoma, ventral view. Scale line = 0,5 mm.

Fig. 3 in Capalictus, a new subgenus of Lasioglossum Curtis, 1833 from South Africa, with description of three new species (Hymenoptera, Apoidea, Halictidae)

Fig. 3. Lasioglossum (Capalictus) mosselinum (Cockerell, 1945), Ƌ. A. Head. B. Mesoscutum and vertex. C. Propodeum. D. First tergum. E. Metasoma, dorsal view. F. Metasoma, ventral view. Scale line = 0,5 mm.