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Figure 1 in The influence of land use-impacted tributaries on water quality and phytoplankton in the Mooi River, North West Province, South Africa
Figure 1: Catchment area of the Mooi River from its source to the confluence with the Vaal River, showing the position of sampling sites in the main stream (1–8) and in the tributaries (WFS, GM and WS). Different types of land use activities in the catchment are also indicated on the map.
Figure 3 in The influence of land use-impacted tributaries on water quality and phytoplankton in the Mooi River, North West Province, South Africa
Figure 3: Canonical Correspondence Analysis (CCA) of the physico-chemical environmental variables, natural log of the phytoplankton data, and the different sites located in the Mooi River for 2015.
Figure 3 in Macrozoobenthos in an altitudinal gradient in North Patagonian Cautín River (Araucanía Region, Chile)
Figure 3. Correlation matrix for PCA for physical-chemical and biotic parameters for sites studied along the Cautín River.
Figure 1 in Macrozoobenthos in an altitudinal gradient in North Patagonian Cautín River (Araucanía Region, Chile)
Figure 1. Map with sites on the Cautín River included in the present study. Table 1. Geographical location, altitude and classification of the sampling sites on the main course of the Cautín River.
Figure 4 in Macrozoobenthos in an altitudinal gradient in North Patagonian Cautín River (Araucanía Region, Chile)
Figure 4. Results of RDA for physical-chemical and biotic parameters for sites studied along the Cautín River.
Fig. 3 in Comparison of carabid densities in different cover crop species in north Florida
Fig. 3 Number of Selenophorus palliatus found in 2 sunn hemp germplasm lines in plots planted in Mar 2016 in Tallahassee, Florida (mean ± SE; n = 8).
Fig. 2 in Comparison of carabid densities in different cover crop species in north Florida
Fig. 2 Number of predator carabid species found in 2 sunn hemp germplasm lines in plots planted in Mar 2016 in Tallahassee, Florida (mean ± SE; n = 8).
DATASET - Mass Spectrometry - Snake venom proteomics of island and mainland V. ammodytes populations from North Macedonia
<p><strong><span>This DATASET collection includes the mass spectrometry files for proteomics venom investigation of island and mainland <em>V. ammodytes</em> populations from North Macedonia.</span></strong></p> <p><strong><span>Sample list:</span></strong></p> <ol> <li><span>Island - adult - male</span></li> <li><span>Island - adult - female</span></li> <li><span>Island - juvenile</span></li> <li><span>Island - subadult</span></li> <li><span>Mainland - adult</span></li> <li><span>Mainland - subadult</span></li> <li><span>Mainland - juvenile</span></li> </ol> <p><strong><span>Folders 01-07 - BOTTOM-UP PROTEOMICS</span></strong><span>: The venom pools were investigated by the bottom-up "snake venomics" (labelled as SVX) approach and in short: separated by RP-HPLC, followed by SDS-PAGE separation and the single bands were in-gel processed by DTT, IAC and finally o/n tryptic digested. Samples submitted to HPLC-MS/MS. Early peptidic fractions of the first HPLC run were directly submitted to HPLC-MS/MS analytic w/o further gel procession. Folders 01 to 07 include the MS and MS/MS spectra of the <em>V. ammodytes</em> sample pools from different populations. Files are included as RAW and MZML format.</span></p> <p><span>Used instrument: LTQ Orbitrap XL mass spectrometer (Thermo, Bremen, Germany) with an Agilent 1260 HPLC system (Agilent Technologies, Waldbronn, Germany) using a reversed-phase Grace Vydac 218MS C18 (2.1 × 150 mm; 5 </span><span>μ</span><span>m particle size) column.</span></p> <p><span>Modifications: UNIMOD:4 - \"Iodoacetamide derivative.\"</span></p> <p><span>Used protein database: Uniprot_8750_serpentes_CanNIso_2674_entries_220210_cRAP_220210.fasta</span></p>
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. Avicennia bicolor — Sediles 461 (CAS, n = 5): P = 19–22 μm, E = 19–24 μm, P:E = 0.86–0.92. Avicennia germinans — Daniel & Araque 9478 (CAS, n = 2): P = 23 μm, E = 24–25 μm, P:E = 0.92; de Nevers et al. 6554 (CAS, n = 2): P = 25 μm, E = 26–28 μm, P:E = 0.89; Palmer 484 (CAS, n = 1): P = 46 μm, E = 24 μm, P:E = 1.90; Salywon 1188 (CAS, n =4): P = 27–42 μm, E = 24–29 μm, P:E = 0.93–1.75. Avicennia marina subsp. australasica — Moran 28024 (CAS, n = 4): P = 28–41 μm, E = 24–27 μm, P:E = 1.04–1.70.
Figure 2. Physeteroidea indet., MNUL.Pal.100.755a in An unfamiliar physeteroid periotic (Cetacea: Odontoceti) from the German middle-late Miocene North Sea basin at Gross Pampau
Figure 2. Physeteroidea indet., MNUL.Pal.100.755a, fragment of the right tympanic bulla from the upper Langenfeldian (Serravallian– Tortonian boundary) of Gross Pampau. (a) Lateral, (b) medial, (c) dorsal, and (d) ventral view.
Figure 4. Physeteroidea indet., MNUL.Pal.100.755a in An unfamiliar physeteroid periotic (Cetacea: Odontoceti) from the German middle-late Miocene North Sea basin at Gross Pampau
Figure 4. Physeteroidea indet., MNUL.Pal.100.755a, measurements of the periotic bone applied in this paper (see Table 1). (a, b) Ventral, (c) medial, (d, e) dorsal, (f) lateral, and (g) posterior view.
Figure 1 in An unfamiliar physeteroid periotic (Cetacea: Odontoceti) from the German middle-late Miocene North Sea basin at Gross Pampau
Figure 1. Map of the Kieswerke Ohle & Lau company gravel pit. The dots represent significant marine mammal findings that are already published, currently being studied or were mentioned in local media after discovery. (1) Mysticete, found 1984, partial skeleton. (2) Kentriodon hoepfneri KazAEr and Hampe, 2014, found in two parts in 1984 and 1989, partial skeleton with nearly complete vertebral column. (3) Praemegaptera pampauensis Behrmann, 1995, found 1989, nearly complete specimen. (4) Praemegaptera pampauensis, found 1993, partial skeleton. (5) Hoplocetus ritzi Hampe, 2006; found 1997; teeth, vertebrae, and bone fragments from a single dislocated skeleton. (6) Kentriodon hoepfneri, found 2000, partial skeleton. (7) Mysticete, found 2012, partial skeleton. (8) Physeteroidea indet., this paper, found 2014, right periotic accompanied by diverse isolated bone fragments. (9) Mysticete, found 2016, partial skeleton. (10) Otariid pinniped; found 2016; ± complete hind limb, bone fragments, teeth. (11) Ziphiidae indet., found 2017, skull. (12) Mysticete, found 2019, partial skeleton. Extract of the "DigitalerAtlasNord" (ETRS89/UTM zone 32N), State Office for Surveying and Geoinformation of SchleswigHolstein (LVermGeo SH).
Figure 3. Physeteroidea indet., MNUL.Pal.100.755a in An unfamiliar physeteroid periotic (Cetacea: Odontoceti) from the German middle-late Miocene North Sea basin at Gross Pampau
Figure 3. Physeteroidea indet., MNUL.Pal.100.755a, right periotic from the upper Langenfeldian (Serravallian–Tortonian boundary) of Gross Pampau. (a, b) Dorsal, (c) medial, (d) lateral, (e, f) ventral, (g) anterior, and (h) posterior view.
Figure 6 in A new delphinid from the lower Pliocene of the North Sea and the early radiations of true dolphins
Figure 6. Schematic dorsal view of the skull in a series of extant small to medium size delphinids. Based on original photos (in large part kindly provided by Giovanni Bianucci) and Arnold and Heinsohn (1996, for Orcaella brevirostris). All crania scaled at same bizygomatic width. Scale bars = 100 mm.
Figure 3 in A new delphinid from the lower Pliocene of the North Sea and the early radiations of true dolphins
Figure 3. Skull of Pliodelphis doelensis gen. nov., sp. nov. IRSNB M.2330 (holotype): (a) right lateral view and (b) interpretive line drawing. Dotted lines correspond to incomplete elements.
Figure 1 in A new delphinid from the lower Pliocene of the North Sea and the early radiations of true dolphins
Figure 1. Locality maps of Antwerp in the north of Belgium and the Deurganck Dock where the specimen studied here (IRSNB M.2330) was discovered, in the Antwerp harbour, as well as other neighbouring docks and a tunnel where geological sections have been studied. Modified from Bisconti et al. (2017).
Figure 5 in A new delphinid from the lower Pliocene of the North Sea and the early radiations of true dolphins
Figure 5. Schematic dorsal view of the skull in a series of extinct delphinids from the late Miocene and Plio–Pleistocene. Based on photos and drawings in Bianucci (1996, 2013); Fordyce et al. (2002); Aguirre-FernAEndez et al. (2009); Murakami et al. (2014), Kimura and Hasegawa (2020), and photos kindly provided by Mark Bosselaers (for Tursiops oligodon) and Giovanni Bianucci (for Lagenorhynchus harmatuki and Stenella rayi). Dotted lines correspond to incomplete elements. All crania scaled at same width of premaxillary sac fossae. Scale bars = 100 mm.
Figure 2 in First record of the subfamily Sagrinae (Coleoptera: Chrysomelidae) from the Eocene of North America
Figure 2. Body outline of the counterpart of Palaeatalasis monrosi sp. nov., holotype, GR2020/2 (ISEA). Scale bars = 1.0 mm.
Figure 1 in First record of the subfamily Sagrinae (Coleoptera: Chrysomelidae) from the Eocene of North America
Figure 1. Body of the counterpart of Palaeatalasis monrosi sp. nov., holotype, GR2020/2 (ISEA). Scale bars = 1.0 mm.
Figure 4 in A new delphinid from the lower Pliocene of the North Sea and the early radiations of true dolphins
Figure 4. Skull of Pliodelphis doelensis gen. nov., sp. nov. IRSNB M.2330 (holotype): (a) ventral view, lacking the basicranium, (b) posterior view, and (c) anterodorsal view.
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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.