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Figs. 2–5. Hadogenes polytrichobothrius n in New South African Flat Rock Scorpions (Liochelidae: Hadogenes)
Figs. 2–5. Hadogenes polytrichobothrius n.sp., habitus of holotype? and paratype / (AMNH). 2. Dorsal aspect,?. 3. Ventral aspect,?. 4. Dorsal aspect, /. 5. Ventral aspect, /. Scale bars 5 10 mm.
Figs. 12–15. Hadogenes polytrichobothrius n in New South African Flat Rock Scorpions (Liochelidae: Hadogenes)
Figs. 12–15. Hadogenes polytrichobothrius n.sp., carinae, trichobothria and macrosetae on dextral pedipalpal segments of paratype / (AMNH). 12. Femur, dorsal aspect. 13. Patella, dorsal aspect. 14. Patella, external aspect. 15. Patella, ventral aspect. Scale bar 5 5 mm.
Fig. 1 in New South African Flat Rock Scorpions (Liochelidae: Hadogenes)
Fig. 1. Map showing the known distribution of species in the bicolor group of Hadogenes: H. bicolor Purcell, 1899 (square), H. longimanus Prendini, 2001 (cross), H. newlandsi Prendini, 2001 (star), H. polytrichobothrius n.sp. (triangle) and H. soutpansbergensis n.sp. (circle). Contour interval, 500 m.
Figs. 6–11. Hadogenes polytrichobothrius n in New South African Flat Rock Scorpions (Liochelidae: Hadogenes)
Figs. 6–11. Hadogenes polytrichobothrius n.sp., carapace, pectines and sternites of? and / paratypes (AMNH). 6. Carapace,?. 7. Carapace, /. 8. Pectines and basal piece,?. 9. Pectines and basal piece, /. 10. Sternite VII,?. 11. Sternite VII, /. Scale bars 5 5 mm.
Figs. 38–41. Hadogenes soutpansbergensis n in New South African Flat Rock Scorpions (Liochelidae: Hadogenes)
Figs. 38–41. Hadogenes soutpansbergensis n.sp., carinae, trichobothria, and macrosetae on dextral pedipalpal segments of holotype? and paratype / (AMNH). 38. Chela, dorsal aspect,?. 39. Chela, dorsal aspect, /. 40. Chela, external aspect, /. 41. Chela, ventrointernal aspect, /. Scale bar 5 5 mm.
TYPES: Male holotype from Panama: Panama: Parque Nacional Altos de Campana, 1 hectare PANCODING Inventory, 895 m, 8.68333°, -79.92972°, June 14–19, 2007, M. Arnedo, D. Dimitrov, G. Hormiga, F. Labarque, M. Ramírez, deposited in MIUP, PBI_OON 42313; same data, 1 male paratype deposited in MACN-Ar 29895, PBI_OON 42312. ETYMOLOGY: A noun in apposition; in Greek religion and mythology, Pan is the god of the wild natural world, of shepherds, flocks, and mountains, and of hunting and rustic music. He has hindquarters, legs, and horns of a goat, and the name is here employed to note the large mac- rosetae at the eye region of males that resemble the horns in some illustrations of this god. DIAGNOSIS: This is one of the most autapomor- phic species from the Americas; males have the labium fused with the sternum (fig. 34B), small chelicerae, shorter than the endite length, with anterior blunt projections, and directed backward in lateral view (fig. 34D, E); clypeus directed back- ward (fig. 34D); two light areas on the sternum just below the endites (fig. 34B), carapace almost flat in lateral view and two strong macrosetae at the eye region, pointing forward (fig. 34C–E). Other characters of the male palp, such as the presence of two apophyses, also distinguish this species from others (fig. 38D–F). MALE (PBI_OON 42312): Total length 1.00. Habitus as in figure 34A–C. CEPHALOTHO- RAX: Carapace orange, with brown stripe along in Taxonomic Revision Of The Jumping Goblin Spiders Of The Genus Orchestina Simon, 1882, In The Americas (Araneae: Oonopidae)
TYPES: Male holotype from Panama: Panama: Parque Nacional Altos de Campana, 1 hectare PANCODING Inventory, 895 m, 8.68333°, -79.92972°, June 14–19, 2007, M. Arnedo, D. Dimitrov, G. Hormiga, F. Labarque, M. Ramírez, deposited in MIUP, PBI_OON 42313; same data, 1 male paratype deposited in MACN-Ar 29895, PBI_OON 42312. ETYMOLOGY: A noun in apposition; in Greek religion and mythology, Pan is the god of the wild natural world, of shepherds, flocks, and mountains, and of hunting and rustic music. He has hindquarters, legs, and horns of a goat, and the name is here employed to note the large mac- rosetae at the eye region of males that resemble the horns in some illustrations of this god. DIAGNOSIS: This is one of the most autapomor- phic species from the Americas; males have the labium fused with the sternum (fig. 34B), small chelicerae, shorter than the endite length, with anterior blunt projections, and directed backward in lateral view (fig. 34D, E); clypeus directed back- ward (fig. 34D); two light areas on the sternum just below the endites (fig. 34B), carapace almost flat in lateral view and two strong macrosetae at the eye region, pointing forward (fig. 34C–E). Other characters of the male palp, such as the presence of two apophyses, also distinguish this species from others (fig. 38D–F). MALE (PBI_OON 42312): Total length 1.00. Habitus as in figure 34A–C. CEPHALOTHO- RAX: Carapace orange, with brown stripe along
Spreadsheet validation for Flat slabs in eccentric punching shear experimental database and analysis
<p>Eccentric punching shear can occur in concrete slab-column connections when the connection is subjected to shear and unbalanced moments. Unbalanced moments occur in all floor slabs at the edge and corner columns. As such, this problem is of practical relevance. However, most punching experiments in the literature deal with concentric punching shear at internal columns. This paper presents a developed database of 128 experiments of flat slabs under eccentric punching shear, including a summary of the testing procedure of each reference and a description of the slab specimens. Additionally, a linear finite element analysis of all the specimens is included to determine the relevant sectional shear forces and moments. Finally, the ultimate shear stresses from the database experiments are compared to the shear capacities determined with ACI 318-19, Eurocode 2, and the Model Code 2010. The comparison shows that the Model Code 2010 is the most precise in the predictions with an average tested-to-predicted ratio of 0.82 and a coefficient of variation of 29.63%. It can be concluded that improvements to the current design methods for eccentric punching shear are necessary.</p>
Spreadsheet for Flat slabs in eccentric punching shear: experimental database and analysis
<p>Eccentric punching shear can occur in concrete slab-column connections when the connection is subjected to shear and unbalanced moments. Unbalanced moments occur in all floor slabs at the edge and corner columns. As such, this problem is of practical relevance. However, most punching experiments in the literature deal with concentric punching shear at internal columns. This paper presents a developed database of 128 experiments of flat slabs under eccentric punching shear, including a summary of the testing procedure of each reference and a description of the slab specimens. Additionally, a linear finite element analysis of all the specimens is included to determine the relevant sectional shear forces and moments. Finally, the ultimate shear stresses from the database experiments are compared to the shear capacities determined with ACI 318-19, Eurocode 2, and the Model Code 2010. The comparison shows that the Model Code 2010 is the most precise in the predictions with an average tested-to-predicted ratio of 0.82 and a coefficient of variation of 29.63%. It can be concluded that improvements to the current design methods for eccentric punching shear are necessary.</p>
Flat oyster (Ostrea edulis) in IMTA with abalone and seaweed: growth and survival
<p>Growth and survival of flat oysters (<em>Ostrea edulis</em>) grown in co-culture (IMTA) with abalone and seaweed in a sea-based system in Aber Wrac'h estuary (Bretagne, France). </p>
Lipid membrane simulations with flat-bottom and double-bilayer setups, part 2/2
<p>To cite: Biriukov, D. and Javanainen, M. Efficient Simulations of Solvent Asymmetry Across Lipid Membranes Using Flat-Bottom Restraints. J. Chem. Theory Comput. 2023, 19 (18), 6332–6341. DOI: <a href="https://doi.org/10.1021/acs.jctc.3c00614">10.1021/acs.jctc.3c00614</a></p> <p>Gromacs molecular dynamics simulations to compare membrane and solvent properties from lipid membrane simulations with flat-bottom and double-bilayer setups. CHARMM36 force field was used except for simulations with peptides, where a prosECCo model was used [Nencini et al., Biophys. J. 121, 157a (2022)]</p> <p>This dataset contains only double-bilayer simulations. The flat-bottom simulations together with all topologies and mdp files can be found in part 1 : DOI: <a href="https://zenodo.org/record/7973838">10.5281/zenodo.7973838</a></p> <p>Abbreviations in the names of simulation files:</p> <ul> <li>"fb" - simulations with a flat-bottom setup</li> <li>"2m" - simulations with two lipid membranes, i.e., a double-bilayer setup</li> <li>"popc" - membrane is modeled as a POPC lipid bilayer</li> <li>"mix" - a realistic membrane with various lipids is modeled, resembling the composition from [Lorent et al., Nat. Methods 16, 644–652 (2020)]</li> <li>"nak" - only sodium and potassium cations, together with chloride anions, are present in the system</li> <li>"ext" - as "nak", but also calcium and magnesium cations are added</li> <li>"r9" - as "nak" but also R9 (nona-arginine) peptides are added on both sides of the membrane</li> <li>"r9k" - as "nak" but also R9 (nona-arginine) peptides are added on the extracellular side of the membrane</li> <li>"one" - ions are present only on one side of a lipid membrane</li> <li>"freecl" - flat-bottom simulations but without restraints on chloride anions</li> <li>"s" - simulations were performed using the scaled-charge prosECCo75 force field based on CHARMM [Nencini et al., Biophys. J. 121, 157a (2022)]</li> <li>"restr" - restraint .gro file with ionic/peptide <em>z</em> coordinates set to zero</li> </ul>
Lipid membrane simulations with flat-bottom and double-bilayer setups, part 1/2
<p>To cite: Biriukov, D. and Javanainen, M. Efficient Simulations of Solvent Asymmetry Across Lipid Membranes Using Flat-Bottom Restraints. J. Chem. Theory Comput. 2023, 19 (18), 6332–6341. DOI: <a href="https://doi.org/10.1021/acs.jctc.3c00614">10.1021/acs.jctc.3c00614</a></p> <p>Gromacs molecular dynamics simulations to compare membrane and solvent properties from lipid membrane simulations with flat-bottom and double-bilayer setups. CHARMM36 force field was used except for simulations with peptides, where a prosECCo model was used [Nencini et al., Biophys. J. 121, 157a (2022)]</p> <p>This dataset contains all the topologies and flat-bottom simulation files. The double-bilayer simulation files can be found in part 2: DOI: <a href="https://zenodo.org/record/7974633">10.5281/zenodo.7974633</a></p> <p>Abbreviations in the names of simulation files:</p> <ul> <li>"fb" - simulations with a flat-bottom setup</li> <li>"2m" - simulations with two lipid membranes, i.e., a double-bilayer setup</li> <li>"popc" - membrane is modeled as a POPC lipid bilayer</li> <li>"mix" - a realistic membrane with various lipids is modeled, resembling the composition from [Lorent et al., Nat. Methods 16, 644–652 (2020)]</li> <li>"nak" - only sodium and potassium cations, together with chloride anions, are present in the system</li> <li>"ext" - as "nak", but also calcium and magnesium cations are added</li> <li>"r9" - as "nak" but also R9 (nona-arginine) peptides are added on both sides of the membrane</li> <li>"r9k" - as "nak" but also R9 (nona-arginine) peptides are added on the extracellular side of the membrane</li> <li>"one" - ions are present only on one side of a lipid membrane</li> <li>"freecl" - flat-bottom simulations but without restraints on chloride anions</li> <li>"s" - simulations were performed using the scaled-charge prosECCo75 force field based on CHARMM [Nencini et al., Biophys. J. 121, 157a (2022)]</li> <li>"restr" - restraint .gro file with ionic/peptide <em>z</em> coordinates set to zero</li> </ul> <p> </p>
Data, Scripts underlying the publication: Identifying the critical turbidity threshold to maintain estuarine tidal flats worldwide
<p>Data & Scripts featured in the currently unpublished manuscript (as of 21-07-2023) Grandjean et al.: 'Identifying the critical turbidity threshold to maintain estuarine tidal flats worldwide'. This study explores the relationship between tidal range and turbidity concentrations on the morphological trajectory of unvegetated tidal flats at a global scale. These files include the scripts used to produce digital elevation models per estuary.</p> <p> </p>
Ramp-Flat and Splay Faulting Illuminated by Frictional Afterslip Following the 2017 Mw 7.3 Sarpol-e Zahab Earthquake
<p>The postseismic InSAR data used in the manuscript "Frictional Afterslip along a Complex Fault Structure Following the 2017 Mw 7.3 Sarpol-e Zahab Earthquake Revealed by InSAR and 2-D Finite Element Models".</p>
"It was recorded on Sunday, morning of the 28th of September as some of the slower runners of the Berlin Marathon made it past Torstrasse near my flat. Iwas out to buy some bread for breakfast, but Iusually bring a camera and my Edirol R-1 recorder whenever Igo out. Since Iwas freshly returned to Berlin Iguess Iwas sensitive to the more antiquated sounds which still survive there, like that of the organ grinder. Iam generally interested in how human beings are replacing the presence of Nature with an artificial environment made entirely by human hands (and thus far more understandable, it is hoped). In this new Human Nature, the sounds of Nature are also Human made. Iwrite about these things, but Ialso use the sounds in my videos and my interactive and generative media work, so generally Iam wandering around building up my archive of media documents for use as material in future works." [Baruch/ gottlieb]17 in Collecting Sounds. Online Sharing of Field Recordings as Cultural Practice
"It was recorded on Sunday, morning of the 28th of September as some of the slower runners of the Berlin Marathon made it past Torstrasse near my flat. Iwas out to buy some bread for breakfast, but Iusually bring a camera and my Edirol R-1 recorder whenever Igo out. Since Iwas freshly returned to Berlin Iguess Iwas sensitive to the more antiquated sounds which still survive there, like that of the organ grinder. Iam generally interested in how human beings are replacing the presence of Nature with an artificial environment made entirely by human hands (and thus far more understandable, it is hoped). In this new Human Nature, the sounds of Nature are also Human made. Iwrite about these things, but Ialso use the sounds in my videos and my interactive and generative media work, so generally Iam wandering around building up my archive of media documents for use as material in future works." [Baruch/ gottlieb]17
Eastern bettong (Bettongia gaimardi) reintroduced to Mulligan's Flat Woodland Sanctuary and Tidbinbilla Nature Reserve: DArT SNPs + individual information
Open the record for dataset details and reuse information.
Animal metacommunities of temporary ponds in a flat grassland landscape of Uruguay
Open the record for dataset details and reuse information.
Koyukuk Flats: soil temperatures at different depths from 2008-2009
This dataset contains soil temperature data from a collapse-scar bog chronosequence at Koyukuk Flats National Wildlife Refuge in western interior Alaska. Temperature sensors were installed at the ground surface and deeper in the soil profile (20-45 cm below the moss surface). These data can be sorted by site, month, day, and depth of measurement.
MCR LTER: Coral Reef: Sand Flat Sampling: Sand Infaunal Surveys
These data represent abundances of infaunal invertebrates in lagoonal sand flats along the north shore of Moorea. Surveys were conducted once along five transects in the Vaipahu lagoon within the LTER 1 study site. The number of individuals from distinct invertebrate taxa were counted from 1815 cubic centimeter sand cores taken at varying distances from a large patch reef. The data also include sand grain size distributions.
Water column chlorophyll concentrations associated with clam flat surveys during year 2010 in the Plum Island Sound estuary, Newbury, Rowley and Ipswich, MA.
Six to eight sites in the Plum Island Sound estuary , the mainstem of the Parker River and Rowley River, in areas close to where other clam samples were being taken for other studies, were selected for monthly chlorophyll sampling to determine the concentration of phytoplankton at these sites.
Sediment grain characteristics and clam densities for clam flat surveys during 2010 in the Plum Island Sound estuary, Newbury, Rowley and Ipswich, MA.
In 2010 a study was conducted at five sites in the Rowley and Parker Rivers, Northeast Massachusetts, to determine the distribution and density of soft shell clams along a transect from the high to low tide line, as well as the sediment grain size distribution a t each of the sites.
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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)
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.