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DALROMS-NWA12 v1.0, a coupled circulation-sea ice-biogeochemistry model for the northwest North Atlantic: output files (2 of 2)
<p>DALROMS-NWA12 v1.0 is a coupled circulation-sea ice-biogeochemistry modelling system based on ROMS, CICE, and MCT. The model domain covers the North Atlantic Ocean from ~81 deg W to ~39 deg W and ~33.5 deg N to 76 deg N. This record includes daily-mean output of all (ocean circulation, sea ice, and biogeochemistry) modules for September 2015. Similar files for September 2013 are available at <a href="https://doi.org/10.5281/zenodo.12744506" target="_blank" rel="noopener">https://doi.org/10.5281/zenodo.12744506</a>.</p> <p>Model codes, scripts for compiling the model, and sample CPP header files and runtime parameter files (namelists) for physics-only simulations are available at <a href="https://doi.org/10.5281/zenodo.12752091" target="_blank" rel="noopener">https://doi.org/10.5281/zenodo.12752091</a>. CPP header and runtime parameter files for the biogeochemistry module are available upon request.</p> <p>Sample input files for physics-only simulations are available at <a href="https://doi.org/10.5281/zenodo.12752190" target="_blank" rel="noopener">https://doi.org/10.5281/zenodo.12752190</a>, <a href="https://doi.org/10.5281/zenodo.12734049" target="_blank" rel="noopener">https://doi.org/10.5281/zenodo.12734049</a>, and <a href="https://doi.org/10.5281/zenodo.12735153" target="_blank" rel="noopener">https://doi.org/10.5281/zenodo.12735153</a>. Input files for the biogeochemistry module are available upon request.</p>
Fig. 3. Tallies within each Tennessee county indicate the total buprestid species recorded from specimen label records spanning 1934 in Seasonal flight activity and distribution of metallic woodboring beetles (Coleoptera: Buprestidae) collected in North Carolina and Tennessee
Fig. 3. Tallies within each Tennessee county indicate the total buprestid species recorded from specimen label records spanning 1934 to 2013. When presented across Tennessee, species yields indicate areas of greatest and least collection activity and highlight regions of future collection interest. This figure is displayed in color online at http://purl.fcla.edu/fcla/entomologist/browse
Fig. 1B in Seasonal flight activity and distribution of metallic woodboring beetles (Coleoptera: Buprestidae) collected in North Carolina and Tennessee
Fig. 1B. Seasonal flight activities recorded for Agrilinae (Coraebini and Trachyini), Polycestinae, and Chrysocrhoinae metallic woodboring beetle species collected across North Carolina (1901–2013) and Tennessee (1934–2013). Collection records frequently included trapping yield results from multi-day deployments; thus, data for individual specimens were pooled within 1 of 4 weeks for each month. Dated records for specimens with labels that noted specimen emergence from infested trunk, stem, firewood, and branch sections are not included within the seasonal ranges presented. Dashed vertical lines (at May and Jul) indicate approximate flight activity period (in North Carolina) for Cerceris fumipennis (Say) (Hymenoptera: Crabronidae) wasps. Asterisks indicate species collected by the wasps during biosurveillance in North Carolina (Nalepa et al. 2013; Swink et al. 2013, 2014). This figure is displayed in color online at http://purl.fcla.edu/fcla/entomologist/browse
Fig. 1C in Seasonal flight activity and distribution of metallic woodboring beetles (Coleoptera: Buprestidae) collected in North Carolina and Tennessee
Fig. 1C. Seasonal flight activities recorded for Buprestinae metallic woodboring beetle species collected across North Carolina (1901–2013) and Tennessee (1934–2013). Collection records frequently included trapping yield results from multi-day deployments; thus, data for individual specimens were pooled within 1 of 4 weeks for each month. Dated records for specimens with labels that noted specimen emergence from infested trunk, stem, firewood, and branch sections are not included within the seasonal ranges presented. Dashed vertical lines (at May and Jul) indicate approximate flight activity period (in North Carolina) for Cerceris fumipennis (Say) (Hymenoptera: Crabronidae) wasps. Asterisks indicate species collected by the wasps during biosurveillance in North Carolina (Nalepa et al. 2013; Swink et al. 2013, 2014). This figure is displayed in color online at http://purl.fcla.edu/fcla/entomologist/browse
Fig. 1A in Seasonal flight activity and distribution of metallic woodboring beetles (Coleoptera: Buprestidae) collected in North Carolina and Tennessee
Fig. 1A. Seasonal flight activities recorded for Agrilinae: Agrilini metallic woodboring beetle species collected across North Carolina (1901–2013) and Tennessee (1934–2013). Collection records frequently included trapping yield results from multi-day deployments; thus, data for individual specimens were pooled within 1 of 4 weeks for each month. Dated records for specimens with labels that noted specimen emergence from infested trunk, stem, firewood, and branch sections are not included within the seasonal ranges presented. Dashed vertical lines (at May and Jul) indicate approximate flight activity period (in North Carolina) for Cerceris fumipennis (Say) (Hymenoptera: Crabronidae) wasps. Asterisks indicate species collected by the wasps during biosurveillance in North Carolina (Nalepa et al. 2013; Swink et al. 2013, 2014). This figure is displayed in color online at http://purl.fcla.edu/fcla/entomologist/browse
Fig. 2. Tallies within each North Carolina county indicate the total buprestid species recorded from specimen label records spanning 1901 in Seasonal flight activity and distribution of metallic woodboring beetles (Coleoptera: Buprestidae) collected in North Carolina and Tennessee
Fig. 2. Tallies within each North Carolina county indicate the total buprestid species recorded from specimen label records spanning 1901 to 2013. When presented across North Carolina, species yields indicate areas of greatest and least collection activity and highlight regions of future collection interest. This figure is displayed in color online at http://purl.fcla.edu/fcla/entomologist/browse
Fig. 1 in Field host range of Apanteles opuntiarum (Hymenoptera: Braconidae) in Argentina, a potential biocontrol agent of Cactoblastis cactorum (Lepidoptera: Pyralidae) in North America
Fig. 1. Distribution of Apanteles opuntiarum (circles) and Apanteles alexanderi (triangles) that emerged from species of Pyralidae collected in Argentina, Aug 2007–Mar 2014.
Figs. 1–10. Verrucoentomon species. 1-3. V in Review of North American Verrucoentomon species (Protura: Acerentomidae, Nipponentominae), with a key to species of the related genus Imadateiella Rusek
Figs. 1–10. Verrucoentomon species. 1-3. V. canadense (Tuxen, 1955). Holotype. 1. Tergite VII, right part; 2. Foretarsal seta δ4; 3. Anterior part of metasternum. Arrows indicate pores (psm = tergal posterosubmedial, psl = tergal posterosublateral pore, sc = sternal central). Scale bar: 20 µm. 4–10. Verrucoentomon imadatei (Nosek, 1977). 4. Hind margin of head; 5. Pseudoculus with cephalic setae l3, sd4 and sd5; 6. Pronotum and mesonotum, right side; 7. Tergite I, right side; 8. Anterior part of prosternum; 9. Anterior part of mesosternum; 10. Sternite VII. Arrows indicate pores (sl = tergal sublateral, al = tergal anterolateral, psm = tergal posterosubmedial, sc = sternal central, spm = sternal posteromedial). Scale bars: 20 µm.
Figs. 11–27 in Review of North American Verrucoentomon species (Protura: Acerentomidae, Nipponentominae), with a key to species of the related genus Imadateiella Rusek
Figs. 11–27. Imadateiella mixta (Nosek, 1977). 11. Hind margin of head; 12. Pseudoculus with setae l3 and sd4; 13. Cephalic seta sd5; 14. Maxillary palp; 15. Labial palp; 16. Foretarsal seta Β1; 17. Foretarsal setae δ4 and δ5; 18. Setae P1a and P2a on mesonotum; 19. Anterior part of mesosternum; 20. Seta A2 on mesosternum; 21. Tergite I, right side; 22. Sternite I; 23. Sternite VII; 24. Seta P1a on sternite VII; 25. Comb; 26. Part of male squama genitalis; 27. Acrostylus of female squama genitalis. Arrows indicate pores (al = tergal anterolateral, psm = tergal posterosubmedial, sc = sternal central, sal = sternal anterolateral, spm = sternal posteromedial, spsm = sternal posterosubmedial). Scale bars: 20 µm.
Figs. 1–3. Myrmecina species. 1 in A new species of Myrmecina (Hymenoptera: Formicidae) from southeastern North America
Figs. 1–3. Myrmecina species. 1. Myrmecina cooperi sp. nov., worker. Length of ant 1.90 mm. 2. Myrmecina americana Emery, worker. Length of ant 2.65 mm. 3. Myrmecina, undescribed species of Fisher & Cover (2007). Length of ant 2.45 mm.
FIGURE 1 in Avicennia (Acanthaceae: Avicennioideae) in North America and Mesoamerica
FIGURE 1 (left). Pollen of Avicennia spp. A–C. Avicennia bicolor (Sediles 461). A. Interapertural view. B. Apertural view. C. Polar view. D–G. Avicennia germinans (D, Palmer 484; E–G, Salywon 1188). D. Interapertural view. E. Apertural view. F. Polar view. G. Interapertural view. H–K. Avicennia marina subsp. australasica (Moran 28024). H. Interapertural view. I. Apertural view. J. Polar view. K. Apertural view. Scales = 5 µm. Pollen measurements (n = number of grains measured, P = polar diameter, and E = equatorial diameter). Many additional grains from each specimen were examined, but data summarized below were made on a subset of those oriented to permit accurate measurements and photographic documentation.
Fig. 3 in The systematics of Late Jurassic tyrannosauroid theropods from Europe and North America
Fig. 3. Autapomorphies of tyrannosauroids Juratyrant langhami Benson, 2008, Kimmeridge Clay, Dorset England, Late Jurassic (early Tithonian) (A, B) and Stokesosaurus clevelandi Madsen, 1974, Morrison Formation, Utah, USA, Late Jurassic (early Tithonian) (C). A. Right pubis (OUMNH J.3311−22) in lateral view, with the autapomorphic lateral fossa denoted. B. Left ischium (OUMNH J.3311−25) in lateral (B1) and anterior (B2) views, with an inset close up (2.5× magnification) of the autapomorphic folded proximal region of the ischial apron (B3). The autapomorphic convex ischial tubercle is also denoted. C. Pubic peduncle of the left ilium (UMNH 2938) in medial view, with the autapomorphic swollen rim indicated.
Fig. 2 in The systematics of Late Jurassic tyrannosauroid theropods from Europe and North America
Fig. 2. The phylogenetic relationships of tyrannosauroids, based on a revised analysis of the Brusatte et al. (2010) dataset. Details of the analysis are described in the text and the dataset is presented in SOM. The cladogram shown here is the single most parsimonious tree recovered by the analysis, with the wildcard taxon Aviatyrannis excluded (570 steps, CI = 0.640, RI = 0.835). Numbers next to nodes denote bootstrap percentages (based on 1000 replicates) and Bremer support. Note that Stokesosaurus clevelandi and "S." langhami (here referred to by its new genus name, Juratyrant) are not found as sister taxa, and therefore a monophyletic Stokesosaurus is not recovered. When Aviatyrannis is included in the analysis, the strict consensus of nine most parsimonious trees (not figured) shows identical and fully resolved relationships among Xiongguanlong and all more derived taxa. However, Stokesosaurus clevelandi, "S." langhami, and Eotyrannus, form a polytomy. This clade, in turn, is part of a large basal polytomy that also includes the Xiongguanlong + more derived clade, Dilong, Aviatyrannis, Guanlong, Kileskus, Proceratosaurus, and Sinotyrannus. On the figured cladogram, the following unambiguous synapomorphies support major clades, with character numbering following that in the character list of Brusatte et al. (2010) and SOM: all tyrannosauroids more derived than Dilong (33, 41, 49, 80, 180, 181, 196, 198, 221, 239, 241, 244, 257, 274, 281, 289, 290); the clade of S. clevelandi, Juratyrant, and Eotyrannus (258, 310, 311, 313); the clade of Juratyrant and Eotyrannus (no unambiguous synapomorphies).
Fig. 1 in The systematics of Late Jurassic tyrannosauroid theropods from Europe and North America
Fig. 1. Ilia of basal non−tyrannosaurid tyrannosauroids with a posterodorsally inclined ridge on the lateral surface of the ilium. A. Right ilium (reversed) of Juratyrant langhami Benson, 2008 (OUMNH J.3311−21), Kimmeridge Clay, Dorset England, Late Jurassic (early Tithonian). B. Left ilium of Stokesosaurus clevelandi, Madsen 1974 (UMNH VP 7473), Morrison Formation, Utah, USA, Late Jurassic (early Tithonian). C. Left ilium of Eotyrannus lengi Hutt, Naish, Martill, Barker, and Newberry, 2001 (MIWG 1997.550), Wessex Formation, Isle of Wight, England, Early Cretaceous (Barremian). All in lateral view. Arrows denote the lateral ridge.
Fig. 37 in Systematic Revision Of The Troglomorphic North American Scorpion Family Typhlochactidae (Scorpiones: Chactoidea)
Fig. 37. Typhlochactas sissomi Francke et al., 2009, subadult ³ holotype (IBUNAM), sinistral pedipalp femur (A) and patella (B–D) showing carinae and distribution of trichobothria. A, B. Dorsal aspect. C. External aspect. D. Ventral aspect. Scales 5 0.5 mm.
Fig. 36 in Systematic Revision Of The Troglomorphic North American Scorpion Family Typhlochactidae (Scorpiones: Chactoidea)
Fig. 36. Typhlochactas sissomi Francke et al., 2009, subadult ³ holotype (IBUNAM), sinistral pedipalp chela showing carinae and distribution of trichobothria. A. Dorsal aspect. B. External aspect. C. Ventral aspect. Scale 5 0.5 mm.
Fig. 40 in Systematic Revision Of The Troglomorphic North American Scorpion Family Typhlochactidae (Scorpiones: Chactoidea)
Fig. 40. Typhlochactas sylvestris Mitchell and Peck, 1977, holotype ♀ (AMNH), sinistral pedipalp femur (A) and patella (B–D) showing carinae and distribution of trichobothria. A, B. Dorsal aspect. C. External aspect. D. Ventral aspect. Scales 5 0.1 mm.
Fig. 39 in Systematic Revision Of The Troglomorphic North American Scorpion Family Typhlochactidae (Scorpiones: Chactoidea)
Fig. 39. Typhlochactas sylvestris Mitchell and Peck, 1977, holotype ♀ (AMNH), sinistral pedipalp chela showing carinae and distribution of trichobothria. A. Dorsal aspect. B. External aspect. C. Ventral aspect. Scale 5 0.1 mm.
Fig. 27. Typhlochactas mitchelli Sissom, 1988 in Systematic Revision Of The Troglomorphic North American Scorpion Family Typhlochactidae (Scorpiones: Chactoidea)
Fig. 27. Typhlochactas mitchelli Sissom, 1988, holotype ³ (AMNH), sinistral pedipalp chela showing carinae and distribution of trichobothria. A. Dorsal aspect. B. External aspect. C. Ventral aspect. Scale 5 0.1 mm.
Fig. 33. Typhlochactas rhodesi Mitchell, 1968 in Systematic Revision Of The Troglomorphic North American Scorpion Family Typhlochactidae (Scorpiones: Chactoidea)
Fig. 33. Typhlochactas rhodesi Mitchell, 1968, holotype ♀ (AMNH), sinistral pedipalp chela showing carinae and distribution of trichobothria. A. Dorsal aspect. B. External aspect. C. Ventral aspect. Scale 5 0.5 mm.
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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.