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Figure 3 in Merluccius polli and M. senegalensis (Merlucciidae) as first records from the Canary Islands (north-eastern Atlantic), with morphology data
Figure 3. – Radiographs of M. senegalensis from the Canary Islands (TFMCBM-VP/01449, adult, 804 mm TL). Insert: Detail of five cervical vertebrae.
Figure 2 in Merluccius polli and M. senegalensis (Merlucciidae) as first records from the Canary Islands (north-eastern Atlantic), with morphology data
Figure 2. – Radiographs of M. polli from the Canary Islands (TFMCBM-VP/01952, maturing female, 624 mm TL). Insert: Detail of five cervical vertebrae.
Figure 1 in Merluccius polli and M. senegalensis (Merlucciidae) as first records from the Canary Islands (north-eastern Atlantic), with morphology data
Figure 1. – The Canary Islands. Collection locations for the first records. Ì: Merluccius polli; ■: Merluccius senegalensis.
Data for sensitivity analysis of Hübler, M., M. Wiese, M. Braun and J. Damster (2023): The distributional effects of CO2 pricing at home and at the border on German income groups
<p>This dataset contains the output files used in the sensitivity analysis of the computable general equilibrium (CGE) model developed in Hübler et al. (2023). Each folder is labeled with the respective set of sector-level elasticity of substitution parameters considered in the analysis: elasticities between domestically produced versus imported goods (esubd), Armington elasticities (esubm) and elasticities between production factors (esubva).</p> <p>For each set of parameters, we generate 1000 random draws from a +-10 % interval around each of the sector-specific elasticities, resulting in 1000 sets of sectoral parameter values. Each .xlsx output file located in a dedicated subfolder corresponds to a model run with a specific set of parameter values. In addition, we conduct sensitivity analyses of two individual parameters, namely the CO2 target (CO2factor) considered in our policy scenarios and the elasticity of substitution in consumption (esub_cons).</p> <p>The sensitivity analysis is carried out using the <a href="https://snakemake.readthedocs.io/en/stable/">Snakeflow</a> workflow management system, and R code for generating parameter spaces and processing the output files is available on <a href="https://github.com/mariuslbraun/climate-trade-distribution-sensitivity">GitHub</a>.</p>
Fig. 1 in New Species Of Pachyrhynchus Germar, 1824 And M Acro Cyrtus H Eller, 1912 (C Oleop Tera: Curculionidae) From The Marinduque Island (Philippines) As A New Example Of Mimetic Species Pair
Fig. 1. Pachyrhynchus rukmaneae sp. n. (A – habitus, dorsal view, B – habitus, lateral view, C – aedeagus (1 – lateral view, 2 – lamella, dorsal view)).
Figura 4. A-M in Cyperaceae nos campos de natureza de Cametá, Pará, Amazônia, Brasil
Figura 4. A-M. Vista lateral das núculas: A. Bulbostylis conifera (A. Gil et al. 798 - MG); B. B. junciformis (C. L. Braga-Silva et al. 67 - MG); C. B. lanata (A. J. Fernandes-Júnior et al. 619 - MG); D. Calyptrocarya glomerulata, com utrículo evidente (C. L. Braga-Silva et al. 111- MG); E. C. montesii, com utrículo evidente (C. L. Braga-Silva et al. 123 - MG); F. Cyperus aggregatus (C. L. Braga-Silva et al. 30 - MG); G. C. haspan (A. Gil et al. 795 - MG); H. C. ligularis (C. L. Braga-Silva et al. 57 - MG); I. C. luzulae (C. L. Braga-Silva et al. 31 - MG); J. C. obtusatus (C. L. Braga-Silva et al. 102 - MG); K. C. sphacelatus (C. L. Braga-Silva et al. 32 - MG); L. C. surinamensis (C. L. Braga-Silva et al. 108 - MG); M. Diplacrum guianense, com hipogínio evidente (C. L. Braga-Silva et al. 106 - MG).
Figura 7. A-M in Cyperaceae nos campos de natureza de Cametá, Pará, Amazônia, Brasil
Figura 7. A-M. Vista lateral das núculas: A. Rhynchospora rugosa, com cerdas perigoniais evidentes (A. J. Fernandes-Júnior et al. 605 – MG); B. R. spruceana (C. L. Braga-Silva et al. 141 - MG); C. R. tenerrima (C. L. Braga-Silva et al. 36 - MG) D. R. aff. tenuis (C. A. S. Silva & F. F. N. S. Lara 661 - MG); E. Scleria amazonica, com hipogínio evidente (C. L. Braga-Silva et al. 162 - MG); F. S. cyperina, com hipogínio evidente (C. L. Braga-Silva et al. 164 - MG); G. S. gaertneri, com hipogínio evidente (C. L. Braga-Silva et al. 125 - MG); H. S. macrophylla, com cúpula evidente (C. L. Braga-Silva et al. 135 - MG); I. S. microcarpa, com cúpula evidente (C. L. Braga-Silva et al. 107 - MG); J. S. mitis, com cúpula evidente (C. L. Braga-Silva et al. 134 - MG); K. S. reticularis, com hipogínio evidente (A. Gil et al. 792 - MG); L. S. tenella (C. A. S. Silva 704 – MG); M. S. violacea, com hipogínio evidente (C. L. Braga-Silva et al. 157 - MG).
Figura 6. A-M in Cyperaceae nos campos de natureza de Cametá, Pará, Amazônia, Brasil
Figura 6. A-M. Vista lateral das núculas: A. Rhynchospora acanthoma, com cerdas perigoniais evidentes (A. J. Fernandes-Júnior et al. 632 - MG); B. R. barbata, com cerdas perigoniais evidentes (C. L. Braga-Silva et al. 16 - MG); C. R. candida (C. A. S. Silva 708 - MG); D. R. cephalotes, com cerdas perigoniais evidentes (K. N. L. Alves et al. 101 - MG); E. R. curvula, com cerdas perigoniais evidentes (C. A. S. Silva & F. F. N. S. Lara 662); F. R. divaricata (C. L. Braga-Silva et al. 128 - MG); G. R. filiformis (C. A. S. Silva 707 - MG); H. R. globosa, com cerdas perigoniais evidentes (A. Gil et al. 765 - MG); I. R. hirsuta (C. L. Braga-Silva et al. 156 - MG); J. R. holoschoenoides, com cerdas perigoniais evidentes (C. L. Braga-Silva et al. 163 - MG); K. R. junciformis (A. Gil et al. 801 - MG); L. R. puber (C. L. Braga-Silva et al. 75 - MG); M. R. riparia (C. L. Braga-Silva et al. 99 - MG).
BSRLC+: An annual land cover dataset for the Baltic Sea Region with crop types and peat bogs at 30 m from 2000 to 2022
<p><strong>(NEW) </strong>Baltic Sea Region Land Cover <em>Urban</em> (BSRLC-U) focusing on urban built-up types now available: <a href="https://zenodo.org/records/17347941">https://zenodo.org/records/17347941 </a></p> <p><strong>Baltic Sea Region Land Cover <em>Plus </em>(BSRLC+) </strong>is annual land cover mapping (30 m) dataset in Europe from 2000 to 2022. The maps contain detailed information of 18 land cover (LC) types, including 9 crop types and 2 peat bog types.</p> <p>Input data : Optical multi-temporal remote sensing imageries (Landsat 5 (TM) / 7 (ETM+) / 8 (OLI) / 9 (OLI+) and Sentinel 2 (A / B ) from 2000 to 2022. Data is processed to surface reflectance and tiled into datacube structure using <a href="https://doi.org/10.3390/rs11091124">Framework for Operational Radiometric Correction for Environmental monitoring - FORCE.</a></p> <p>Mapping method: Maps are produced using data encoding and deep learning classification according to <a href="https://doi.org/10.1016/j.jag.2024.103867">Pham et al. 2024</a></p> <p>Validation: Maps have been rigorously validated using independent in-situ data <a href="https://doi.org/10.1038/s41597-020-00675-z">The Land Use/Cover Area frame Survey (LUCAS)</a>. </p> <p>Traing data and validation data are available: <a href="https://zenodo.org/records/11073291">https://zenodo.org/records/11073291</a></p> <p>This dataset contains:</p> <ul> <li><strong>00_preview.png</strong>: Preview map (2022) of the Baltic Sea region</li> <li><strong>BSRLC_{year}.tif</strong>: Annual map data (30 m) in GeoTIFF format (projection ETRS89 / EPSG:3035)</li> <li><strong>BSRLC_legend.xlss</strong>: Land cover codes and class names</li> <li><strong>BSRLC_qgis_style.qml</strong>: Map style to be used in QGIS</li> <li><strong>BSRLC_arcgis_style.lyrx</strong>: Map style to be used in ArcGIS</li> </ul> <p>Land cover codes (can also be found in <strong>BSRLC_legend.xlss</strong>):</p> <ul> <li>1: Built-up</li> <li>2: Bareland</li> <li>3: Water</li> <li>4: Shrubland</li> <li>5: Broadleaf forest</li> <li>6: Coniferous forest</li> <li>7: Wetland marsh</li> <li>8: Exploited peat bog</li> <li>9: Unexploited peat bog</li> <li>10: Wheat</li> <li>11: Barley</li> <li>12: Rye</li> <li>13: Oat</li> <li>14: Maize</li> <li>15: Seed crops</li> <li>16: Root crops</li> <li>17: Pulses, vegetable</li> <li>18: Grassland</li> <li>255: Nodata</li> </ul> <p> </p> <p><strong>Publication (please cite this publication if you are using the dataset):</strong></p> <ul> <li>Pham, V.-D., de Waard, F., Thiel, F., Bobertz, B., Hellmann, C., Nguyen, D.-V., Beer, F., Arasumani, M., Schwieder, M., Hartleib, J., Frantz, D., & van der Linden, S. (2024). An annual land cover dataset for the Baltic Sea Region with crop types and peat bogs at 30 m from 2000 to 2022. <em>Scientific Data, 11</em>, 1242, <a href="https://doi.org/10.1038/s41597-024-04062-w">https://doi.org/10.1038/s41597-024-04062-w</a></li> </ul> <p> </p> <p><strong>Other related publications:</strong></p> <ul> <li><em>Pham, V.-D., Tetteh, G., Thiel, F., Erasmi, S., Schwieder, M., Frantz, D., & van der Linden, S. (2024). Temporally transferable crop mapping with temporal encoding and deep learning augmentations. International Journal of Applied Earth Observation and Geoinformation, 129, 103867, <a href="https://doi.org/10.1016/j.jag.2024.103867">https://doi.org/10.1016/j.jag.2024.103867</a></em></li> <li><em>Frantz, D. (2019). FORCE—Landsat + Sentinel-2 Analysis Ready Data and Beyond. Remote Sensing, 11, <a href="https://doi.org/10.3390/rs11091124">https://doi.org/10.3390/rs11091124</a></em></li> </ul> <p> </p> <p><strong>Funding</strong></p> <p>This datatset is created in the frame of the Interdisciplinary Research Center for the Baltic Sea Region Research (IFZO) of University of Greifswald, Germany, and the research project Fragmented Transformations, which is funded by the German Federal Ministry of Education and Research (FKZ 01UC2102). </p>
Figs 1, 2. M in Melting the iceberg: A new Megaselia Rondani species (Diptera: Phoridae) from Mali with the most striking wing ornament
Figs 1, 2. M. guentermuelleri sp. n., frontal setation (1) and left side of hypopygium (2). Scale bar = 0.1 mm.
FIG. 32. A and B, Perameles nasuta AMNH M-160199 in Transverse Canal Foramen And Pericarotid Venous Network In Metatheria And Other Mammals
FIG. 32. A and B, Perameles nasuta AMNH M-160199 (Peramelidae, Peramelemorphia), adult caudal cranium in (respectively) ventral and right oblique lateral views. C and D, Perameles nasuta AMNH M-154403, damaged adult caudal cranium, showing (respectively) endocranial floor and closeup of left carotid groove. In A
FIG. 36. A and B, Dipodomys deserti AMNH M-182081 in Transverse Canal Foramen And Pericarotid Venous Network In Metatheria And Other Mammals
FIG. 36. A and B, Dipodomys deserti AMNH M-182081 (Dipodomyinae, Heteromyidae, Rodentia), adult caudal cranium in ventral and endocranial aspects; C, Galago demidovii AMNH M-89605 (Galagidae, Primates), adult caudal cranium in ventral aspect. Despite highly derived aspect of kangaroo rat skull, mesocranial position of foramina for sphenopterygoid veins suggests that latter may arise from emissaria comparable to those giving rise to transverse canal veins in marsupials. In Galago and other lorisiforms, in addition to ascending pharyngeal artery, rostral carotid foramen transmits large vein with same relations as internal carotid vein. Key: bcf, basicapsular fenestra (includes piriform fenestra and carotid foramen; see Brylski, 1990); BO, basioccipital; BS, basisphenoid; ccf, caudal carotid foramen; eam, external acoustic meatus; EC, ectotympanic; fm, foramen magnum; fo, foramen ovale; hf, hypoglossal foramen; hpf, hypophyseal fossa; jf, jugular foramen; pglf, postglenoid foramen; pgli, postglenoid incisure; PS, presphenoid; PT, pterygoid; rcf, rostral carotid foramen; spf, sphenopterygoid foramen (=?transverse canal foramen); stf, stapedial foramen (according to Howell, 1932; Brylski, 1990); tgf, fossa for trigeminal ganglion.
FIG. 28. Sarcophilus laniarius AMNH M-65673 in Transverse Canal Foramen And Pericarotid Venous Network In Metatheria And Other Mammals
FIG. 28. Sarcophilus laniarius AMNH M-65673 (Dasyuridae, Dasyuromorphia), adult caudal cranium in A, ventral, B, oblique lateral, and C, oblique endocranial aspects; and D, S. harrisii, venogram (after Shah and Nicol, 1989: fig. 2). (Although catalogued as S. laniarius, usually regarded as an extinct taxon, AMNH M-65673 came to the AMNH in 1913 from New York Zoological Society, and is therefore more likely S. harrisii.) Note asymmetry within endocranial carotid grooves—caudal branch present on left side only. Plexiform nature of vessels identified in original venogram as internal jugular veins, as well as their apparent medial convergence, suggest that they may instead represent ventral petrosal sinus and its extracranial continuation, seen in anastomotic union with internal vertebral venous plexus. True internal jugular veins are probably situated more laterally (asterisk). Key: A–C: AS, alisphenoid; astp, tympanic process of alisphenoid; ats, sulcus for auditory tube; bjs, basijugular sulcus; BO, basioccipital; BS, basisphenoid; cbf, caudal branch foramen; cchf, caudal condylohypoglossal foramen; eam, external acoustic meatus; EC, ectotympanic; ET, ethmoid; encf, endocranial carotid foramen; encg, endocranial carotid groove; etbs, eminence of transverse basicranial sinus; evpf, foramen for extracranial continuation of ventral petrosal sinus; excf, exocranial carotid foramen; fo, foramen ovale; fr, foramen rotundum; FR, frontal; jf, jugular foramen; onvs, sulcus for ophthalmic neurovascular array; mxns, sulcus for maxillary nerve; pbs, presphenoid-basisphenoid synchondrosis; PE, petrosal;
FIG. 27. Dasyurus hallucatus TMM M-6921 in Transverse Canal Foramen And Pericarotid Venous Network In Metatheria And Other Mammals
FIG. 27. Dasyurus hallucatus TMM M-6921 (Dasyuridae, Dasyuromorphia), adult caudal cranium, selected coronal segments in rostrocaudal order (data source, table 2). In A–C, rostral transverse basisphenoid sinus inflates endocranial surface of basisphenoid, forms compound junction with rostral branches of transverse canals. In D, caudal branch foramina open into endocranium on rostral margin of carotid grooves (arrows). However, as no definite trackway for this vein can be detected, actual course not certain. Key: AS, alisphenoid; astp, tympanic process of alisphenoid; bcf, basicapsular fenestra; BS, basisphenoid;?cbs, assumed track of caudal branch of transverse canal; cc, carotid canal; ctbs, caudal portion of transverse basisphenoid sinus; encf, endocranial carotid foramen; encg, endocranial carotid groove; etbs, eminence of transverse basisphenoid sinus; hpf, hypophyseal fossa; junc, junction of transverse canals; le, lateral extension of transverse basisphenoid sinus; mxns, sulcus for maxillary nerve; onvs, sulcus for ophthalmic neurovascular array; rbtc, rostral branches of transverse canal; rtbs, rostral portion of trans-
FIG. 24. Vombatus ursinus AMNH M-176103 in Transverse Canal Foramen And Pericarotid Venous Network In Metatheria And Other Mammals
FIG. 24. Vombatus ursinus AMNH M-176103 (Vombatidae, Diprotodontia), adult caudal cranium in A, ventral; B, oblique caudolateral, and C, endocranial aspects. In C, RBTC canals are notably large (fig. 25B) and sharply define rostral border of deep hypophyseal fossa. Key: astp, tympanic process of alisphenoid; bjs, basijugular sulcus; BO, basioccipital; BS, basisphenoid; cbf, foramen for caudal branch of transverse canal vein; cc, carotid canal; ccs, exocranial sulcus leading to carotid canal; cchf, caudal condylohypoglossal foramen; cpf, craniopharyngeal foramen; cspf, craniospinal foramen; encg, endocranial carotid groove; etcl, eminence formed by junction of rostral branches of transverse canals; evpf, foramen for extracranial continuation of
FIG. 20. Osphranter robustus AMNH M-80171 in Transverse Canal Foramen And Pericarotid Venous Network In Metatheria And Other Mammals
FIG. 20. Osphranter robustus AMNH M-80171 (Macropodidae, Diprotodontia), juvenile caudal cranium, selected coronal segments in rostrocaudal order (data source, table 2). A–F, Conjectured arrangement of mesocranial blood vessels (red, arterial only; blue, venous only), sizes exaggerated for clarity. Macropodids often have multiple transverse canal foramina (e.g., Notamacropus, fig. 18B). In this specimen, accessory foramina (arrow in A) are tiny and open into cancellous tissue, but do not form recognizable junction or communicate directly with endocranium or much larger main foramen (cf. Trichosurus, fig. 22A, B). Nevertheless, they may qualify as RBTCs. In C–F, external apertures for main transverse canal and carotid canal can be seen passing through floor of endocranial carotid groove, where their pathways merge. As a result there is no separate caudal branch foramen because entire trunk consists of caudal branch vein. Whether it retains its separate identify or anastomoses with internal carotid vein in carotid groove as suggested in C (?icv + cbv) is unknown. In any case, in this reconstruction internal carotid vein is shown as departing as a separate vessel through main transverse canal foramen, as in other taxa. Key: AS, alisphenoid; bbs, basisphenoid-basioccipital synchondrosis; BS, basisphenoid; cbf, caudal branch foramen; cbv, caudal branch vein; cc, carotid canal; cs/ov, opthalmic vein entering cavernous sinus; cs/vps, cavernous sinus releasing ventral petrosal sinus; ctbs, caudal portion of transverse basisphenoid sinus; encf, endocranial carotid foramen; encg, endocranial carotid groove; fo, foramen ovale; hpf, hypophyseal fossa; ica, internal carotid artery; icv, internal carotid vein;?icv + cbv, possible anastomosis of caudal branch vein of transverse canal and internal carotid vein; le, lateral extension of transverse basisphenoid sinus; mca, middle cerebral artery; mxns, suclus for maxillary nerve; oa, ophthalmic artery; ov, ophthalmic vein; PT, pterygoid; ptc, pterygoid canal; rtbs, rostral portion of transverse basisphenoid sinus; SQ, squamosal; tcf, transverse canal foramen; tgf, trigeminal ganglion fossa; ttcv, trunk transverse canal vein; vps, ventral petrosal sinus.
FIG. 35. Notoryctes typhlops AMNH M–202103 in Transverse Canal Foramen And Pericarotid Venous Network In Metatheria And Other Mammals
FIG. 35. Notoryctes typhlops AMNH M–202103 (Notoryctidae, Notoryctemorphia), adult caudal cranium, selected coronal segments in rostrocaudal order (data source, table 2). In A and B, rostral portion of transverse basisphenoid sinus and transverse canal are fully integrated. In C and D, roof of transverse basisphenoid sinus bears a large opening (double asterisks), presumably for a venous connection, although given its rostral location it is probably not related to hypophyseal fossa. In E and F, transverse basicranial sinus continues caudally as a pair of semidistinct large pneumatic chambers. On right side a small tube for caudal branch, originating from carotid canal, opens into ipsilateral chamber, but ends quickly. In G, partition (single asterisk) within carotid canal defines two channels; lateral one leads into small tube in F, medial one into endocranial carotid foramen. Key: astp, tympanic process of alisphenoid; BS, basisphenoid; cbf, caudal branch foramen; cbtc, possible conduit for caudal branch of transverse canal; cc, carotid canal; ccs, sulcus leading into carotid canal; ctbs, caudal portion of transverse basisphenoid sinus; encf, endocranial carotid foramen; hpf, hypophyseal
FIG. 26. Dasyurus hallucatus AMNH M-16033 in Transverse Canal Foramen And Pericarotid Venous Network In Metatheria And Other Mammals
FIG. 26. Dasyurus hallucatus AMNH M-16033 (Dasyuridae, Dasyuromorphia), adult caudal cranium in ventral view. Note large size of piriform fenestra, acting as exit aperture for mandibular nerve in absence of separate foramen ovale. Exocranial aperture of carotid canal cannot be seen adequately in this perspective. Key: astp, tympanic process of alisphenoid; bjs, basijugular sulcus; BO, basioccipital bone; BS, basisphenoid; cchf, caudal condylohypoglossal foramen; eam, external acoustic meatus; evpf, foramen for extracranial continuation of ventral petrosal sinus; excf, exocranial carotid foramen; io + pf, incisura ovalis and piriform fenestra (undivided); jf, jugular foramen; pglf, postglenoid foramen; pr, promontorium of petrosal; ptpf, pterygopalatine fissure; rchf, rostral condylohypoglossal foramen; stmf, stylomastoid foramen; tcf, transverse canal foramen.
FIG. 34. Notoryctes typhlops AMNH M–202103 in Transverse Canal Foramen And Pericarotid Venous Network In Metatheria And Other Mammals
FIG. 34. Notoryctes typhlops AMNH M–202103 (Notoryctidae, Notoryctemorphia), adult caudal cranium in A, ventral, and B, oblique lateral views. In A, note internal subdivision within carotid groove (asterisk), assumed to separate internal carotid neurovascular bundle from channel for caudal branch of transverse canal. Key: astp, tympanic process of alisphenoid; BO, basioccipital; BS, basisphenoid; cspf, craniospinal foramen; eam, external acoustic meatus; evpf, extracranial extention of ventral petrosal sinus; evpf + jf, joint aperture for extracranial extension of ventral petrosal sinus and internal jugular vein; excf, exocranial carotid foramen; fm, foramen magnum; fo, foramen ovale; gf, mandibular fossa; jf, jugular foramen; ptpf, foramen for nerve of pterygoid canal; rchf + cchf, joint aperture for rostral and caudal condylohypoglossal foramina; sof, sphenooccipital fissure; stmf, stylomastoid foramen; tcf, transverse canal foramen; tmc, tympanic cavity.
FIG. 2. Didelphis virginiana AMNH M-217731 in Transverse Canal Foramen And Pericarotid Venous Network In Metatheria And Other Mammals
FIG. 2. Didelphis virginiana AMNH M-217731 (Didelphidae, Didelphimorphia), caudal cranium in A, ventral; B, oblique caudal, and C, endocranial views. In C, only one foramen (for internal carotid neurovascular bundle) opens into endocranial carotid groove, because caudal branch of transverse canal vein and its foramen are not present. Small aperture opening in rostral wall of hypophyseal fossa is cranio-
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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.