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FIG. 7 in The Walker Scale: Details of a Method for Assessing Beach-Spawning Runs of California Grunion Leuresthes tenuis (Atheriniformes: Atherinopsidae)
FIG. 7. Report using Walker Scale in smaller segments, in the context of a coastal construction project. Map of Santa Ana River, California from Merkel & Associates, 2017 (used with permission of Keith Merkel). This would be reported as a W-4 for the Grunion Greeters for 4/12, a W-2 on 4/13, and a W-1 on 4/14. The detailed locations given for the run assist in project management along the shoreline to avoid nest sites during construction.
FIG. 1 in The Walker Scale: Details of a Method for Assessing Beach-Spawning Runs of California Grunion Leuresthes tenuis (Atheriniformes: Atherinopsidae)
FIG. 1. (A) California Grunion spawn out of water on beaches in southern California. Photo by Arnold Liu (used with permission of Grunion.org). (B) Grunion Greeters at a spawning run, scored as W-4. Photo by Harris Lakisic (used with permission of Grunion.org).
Derived seismic data products from paper: "Seismic Imaging of the Reykjanes Peninsular, Iceland: Crustal-scale context of geothermal areas and ongoing volcano-tectonic unrest"
<p>Receiver Functions (RF) and Dispersion Curves derived from seismic stations throughout the Reykjanes Peninsular SW Iceland. </p> <p>RF are in Smurfpy python3 PICKLE format - details on format and scripts to read in here: https://github.com/sannecottaar/smurfpy. Folder <strong> </strong>has the following file structure:</p> <p><strong>RF_Data_Zenodo</strong> --> contains station folders: <strong>Network.Station</strong> --> contains folders <strong>goodRF_crust2</strong> and <strong>goodRF_crust6 </strong>where 2 and 6 refer to Gaussian pulse widths used to produce RF via iterative deconvolution --> contains RF files in format <strong><em>NETWORK.STATION_BAZ_EPIDIST_EVTIME.PICKLE</em></strong> and subfolders of identified highly similar waveform subsets in the format <strong>BAZ_NNN_NNN </strong>used in data inversions<strong><br></strong></p> <p>Dispersion curves are in Fast Marching Surfacewave Tomography FMST input format (Rawlinson and Sambridge, 2005), details on format in FMST manual: https://iearth.edu.au/codes/FMST/instructions.pdf. Folder <strong>FMST_Dispersion_Inputs_Zenodo </strong>contains the following files:</p> <ul> <li>otimes0.25Hz.dat</li> <li>otimes0.2Hz.dat</li> <li>otimes0.35Hz.dat </li> <li>otimes0.3Hz.dat</li> <li>otimes0.45Hz.dat</li> <li>otimes0.4Hz.dat</li> <li>otimes0.5Hz.dat</li> <li>sources.dat </li> <li>receivers.dat</li> </ul> <p> </p> <p><em>References</em>:</p> <div>Rawlinson, Nick. "FMST: fast marching surface tomography package–Instructions." <em>Research School of Earth Sciences, Australian National University, Canberra</em> 29 (2005): 47.</div>
Figure 3 in Detailed integrative taxonomic analysis reveals large-scale species misidentification of barnacles based on DNA barcoding data
Figure 3. Neighbour-joining tree for the three investigated barcode index numbers. Ŋe coloured sequences in each clade indicate our newly generated sequences of specimens with unequivocal morphological identification.
Figure 2 in Detailed integrative taxonomic analysis reveals large-scale species misidentification of barnacles based on DNA barcoding data
Figure 2. Morphology of unidentified Balanus sp. individuals of clade A (BOLD:AAG0069) (A), Balanus balanus (B), Balanus crenatus
Figure 1 in Detailed integrative taxonomic analysis reveals large-scale species misidentification of barnacles based on DNA barcoding data
Figure 1. Bubble plot of the correspondence between species assignments and the barcode index number (BIN; genetic clade). Ŋe size of the bubbles corresponds to the number of sequences contained in each combination of BIN and species assignment. Vertical lines highlight BINs that contain more than one species assignment, and horizontal lines highlight species assignments that are present in more than one BIN. Grey bubbles indicate a one-to-one match between BIN and species assignment. Coloured bubbles represent the three BINs that were investigated further by integrative taxonomic analysis.
Рис. 1. Kellicottia bostoniensis (Rousselet, 1908), партеногенетическая ♀ из Можайского воΔохраниΛища. 1 — внешний виΔ; 2 — панцирь с яйцом; 3 — шипы переΔнего края панциря; 4 — заΔний шип Fig. 1. Kellicottia bostoniensis (Rousselet, 1908), parthenogenetic ♀ from the Mozhaisk Reservoir. 1 — external appearance; 2 — shell with an egg; 3 — spines of the anterior part of shell; 4 — rear spine. Scale: 1 — 250 μm; 2–3 — 150 μm; 4 — 50 μm in Kellicottia Bostoniensis (Rousselet, 1908) (Rotifera: Brachionidae) И Eurycercus Macracanthus Frey, 1973 (Crustacea: Cladocera)
Рис. 1. Kellicottia bostoniensis (Rousselet, 1908), партеногенетическая ♀ из Можайского воΔохраниΛища. 1 — внешний виΔ; 2 — панцирь с яйцом; 3 — шипы переΔнего края панциря; 4 — заΔний шип Fig. 1. Kellicottia bostoniensis (Rousselet, 1908), parthenogenetic ♀ from the Mozhaisk Reservoir. 1 — external appearance; 2 — shell with an egg; 3 — spines of the anterior part of shell; 4 — rear spine. Scale: 1 — 250 μm; 2–3 — 150 μm; 4 — 50 μm
Рис. 2. Eurycercus macracanthus Frey, 1973, партеногенетическая ♀ из Можайского воΔо- храниΛища. 1 — внешний виΔ; 2 — конечность (торакопоΔа) I; 3 — ΔистаΛьная часть по- стабΔомена; 4 — гоΛовная пора; 5 — постабΔомен; 6 — маргинаΛьные зубцы постабΔомена Fig. 2. Eurycercus macracanthus Frey, 1973, parthenogenetic ♀ from the Mozhaisk Reservoir. 1 — external appearance; 2 — extremity (thoracopod) I; 3 — distal part of postabdomen; 4 — ce- phalic pore; 5 — postabdomen; 6 — marginal teeth of postabdomen. Scale: 1 — 500 μm; 2 — 80 μm; 3, 6 — 100 μm; 4 — 20 μm; 5 — 200 μm in Kellicottia Bostoniensis (Rousselet, 1908) (Rotifera: Brachionidae) И Eurycercus Macracanthus Frey, 1973 (Crustacea: Cladocera)
Рис. 2. Eurycercus macracanthus Frey, 1973, партеногенетическая ♀ из Можайского воΔо- храниΛища. 1 — внешний виΔ; 2 — конечность (торакопоΔа) I; 3 — ΔистаΛьная часть по- стабΔомена; 4 — гоΛовная пора; 5 — постабΔомен; 6 — маргинаΛьные зубцы постабΔомена Fig. 2. Eurycercus macracanthus Frey, 1973, parthenogenetic ♀ from the Mozhaisk Reservoir. 1 — external appearance; 2 — extremity (thoracopod) I; 3 — distal part of postabdomen; 4 — ce- phalic pore; 5 — postabdomen; 6 — marginal teeth of postabdomen. Scale: 1 — 500 μm; 2 — 80 μm; 3, 6 — 100 μm; 4 — 20 μm; 5 — 200 μm
Adaptation of the Indonesian Version of the Nomophobia Scale (NMP-Q-10)
<p><span>Nomophobia has become a new issue related to smartphone use. Unfortunately, in Indonesia, there is still a limited availability of valid and reliable measurement tools. This study aimed to test the construct validity of the nomophobia instrument developed by Warsah et al. (2023), which consists of 10 items adapted into Indonesian and subsequently modified by the researchers. Data were obtained from young adults, specifically university students aged 18-24 years in Yogyakarta. A total of 410 respondents participated in this study. Confirmatory factor analysis (CFA) was conducted using Jamovi. Based on the construct validity test results using unidimensional CFA, a model fit was achieved in the first stage by excluding one item (item number 10). The second stage involved using the results from the first stage and renumbering the items, which also yielded a well-fitting model with valid loading factors for all items. The results of this test indicate that the Indonesian version of the nomophobia scale is valid and reliable for use in various settings to accurately measure the level of nomophobia among university students. This data represents the findings from a study of 410 college students.</span></p>
FIGURE 53 in Reassessment of the phylogenetic position of the spiny-scale pricklefish Hispidoberyx ambagiosus (Teleostei: Hispidoberycidae) based on comparative morphology
FIGURE 53. Previously inferred relationships of Berycida and related taxa based on molecular data. A, Miya et al. (2005) and Near et al. (2012); B, Betancur-R et al. (2013, 2017); C, Miya et al. (2003), Chen et al. (2014), Dornburg et al. (2017) and Ghezelayagh et al. (2022).
FIGURE 52 in Reassessment of the phylogenetic position of the spiny-scale pricklefish Hispidoberyx ambagiosus (Teleostei: Hispidoberycidae) based on comparative morphology
FIGURE 52. Previously inferred relationships of Berycida and related taxa based on morphological characters. A, Stiassny & Moore (1992); B, Moore (1993); C, Johnson & Patterson (1993); D, Zehren (1979).
FIGURE 50 in Reassessment of the phylogenetic position of the spiny-scale pricklefish Hispidoberyx ambagiosus (Teleostei: Hispidoberycidae) based on comparative morphology
FIGURE 50. Cladogram and character distribution on clades A to M2. A, ACCTRAN; D, DELTRAN; r, reversal; asterisk, autapomorphy.
FIGURE 48 in Reassessment of the phylogenetic position of the spiny-scale pricklefish Hispidoberyx ambagiosus (Teleostei: Hispidoberycidae) based on comparative morphology
FIGURE 48. Photograph (A) and line drawing (B) of lateral line scales in Hispidoberyx ambagiosus, HUMZ 194634, 180.7 mm SL. Gray shaded processes and dashed lines indicate papillate neuromasts and trunk canals, respectively. Scale indicates 5 mm.
FIGURE 46 in Reassessment of the phylogenetic position of the spiny-scale pricklefish Hispidoberyx ambagiosus (Teleostei: Hispidoberycidae) based on comparative morphology
FIGURE 46. Tominaga's organ in Stephanoberyx monae, HUMZ 230037, 88.8 mm SL. A, lateral aspect of preorbital region after removal of epidermis. B, line drawing of lateral aspect of Tominaga's organ. NR, nasal rosette; TO, Tominaga's organ. Scale indicates 5 mm.
FIGURE 43 in Reassessment of the phylogenetic position of the spiny-scale pricklefish Hispidoberyx ambagiosus (Teleostei: Hispidoberycidae) based on comparative morphology
FIGURE 43. Dorsal aspects of anterior portions of body and carinal muscles in (A) Hispidoberyx ambagiosus, HUMZ 193670, 178.8 mm SL, and (B) Neoniphon sammara, HUMZ 40434, 151.8 mm SL. DPT, distal pterygiophore; ES, extrascapular; PPT, proximal pterygiophore; PT, posttemporal; SCA, supracarinalis anterior; SN, supraneurals. Arrows indicate unnamed muscles. Scales indicate 5 mm.
FIGURE 47 in Reassessment of the phylogenetic position of the spiny-scale pricklefish Hispidoberyx ambagiosus (Teleostei: Hispidoberycidae) based on comparative morphology
FIGURE 47. Lateral aspect of prepectoral organ on right side in Acanthochaenus luetkenii, USNM 307916, 89.1 mm SL. A, prepectoral region medial to opercle. B, after removal of epidermis, connective tissue and gill filaments. C, line drawing of prepectoral organ. D, enlarged view of prepectoral organ. CL, cleithrum; PPO, prepectoral organ; SCL, supracleithrum. Arrows indicate external openings. Scale indicates 3 mm.
FIGURE 49 in Reassessment of the phylogenetic position of the spiny-scale pricklefish Hispidoberyx ambagiosus (Teleostei: Hispidoberycidae) based on comparative morphology
FIGURE 49. Strict consensus tree of three equally parsimonious trees representing phylogenetic relationships of Hispidoberyx ambagiosus and related taxa, with classifications of Berycida sensu Nelson et al. (2016).
FIGURE 44 in Reassessment of the phylogenetic position of the spiny-scale pricklefish Hispidoberyx ambagiosus (Teleostei: Hispidoberycidae) based on comparative morphology
FIGURE 44. Lateral aspect of anterior trunk muscles in Hispidoberyx ambagiosus, HUMZ 193670, 178.8 mm SL. EPAX, epaxialis; ICA, infracarinalis anterior; ICM, infracarinalis medius; LS, lateralis superficialis; OBI, obliquus inferioris; OBS, obliquus superioris; PCE, pharyngoclavicularis externus; SCA, supracarinalis anterior; SH, sternohyoideus. Scale indicates 5 mm.
FIGURE 45 in Reassessment of the phylogenetic position of the spiny-scale pricklefish Hispidoberyx ambagiosus (Teleostei: Hispidoberycidae) based on comparative morphology
FIGURE 45. Tominaga's organ in Hispidoberyx ambagiosus (B–D, HUMZ 194634, 180.7 mm SL; E, HUMZ 193670, 178.8 mm SL). A, diagrammatic illustration indicating position of Tominaga's organ. B, lateral aspect of preorbital region after removal of epidermis. C, dorsal aspect of extracted Tominaga's organ. D, posterior tip of duct after removal of epidermis. E, line drawing of lateral aspect of Tominaga's organ. NR, nasal rosette; TO, Tominaga's organ. B and C, posterior portion of duct is damaged. D shown as mirror image. Arrow indicates tip of duct. Scale indicates 5 mm.
FIGURE 42 in Reassessment of the phylogenetic position of the spiny-scale pricklefish Hispidoberyx ambagiosus (Teleostei: Hispidoberycidae) based on comparative morphology
FIGURE 42. Lateral aspects of (A) dorsal and (B) anal-fin muscles in Hispidoberyx ambagiosus, HUMZ 194634, 180.7 mm SL. DEA, depressores anales; DED, depressores dorsales; ERA, erectores anales; ERD, erectores dorsales; ICM, infracarinalis medius; INA, inclinatores anales; IND, inclinatores dorsales; SCA, supracarinalis anterior. Scales indicate 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.