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130 results for “BITs”
FIGURE 12 in Contributions to the taxonomy of the Irano-Turanian genus Rhabdosciadium (Apiaceae): Nomenclatural notes, carpology, molecular phylogeny and the description of a new species from Bitlis (Turkey)
FIGURE 12. Paniculate corymbose inflorescence (general view and detail) of Rhabdosciadium anatolyi (from the epitype, M. Fırat 30400).
FIGURE 8 in Contributions to the taxonomy of the Irano-Turanian genus Rhabdosciadium (Apiaceae): Nomenclatural notes, carpology, molecular phylogeny and the description of a new species from Bitlis (Turkey)
FIGURE 8. Umbels, fruits, and leaves of Rhabdosciadium hizanense (from the holotype, M. Fırat 32618).
FIGURE 3 in Contributions to the taxonomy of the Irano-Turanian genus Rhabdosciadium (Apiaceae): Nomenclatural notes, carpology, molecular phylogeny and the description of a new species from Bitlis (Turkey)
FIGURE 3. Phylogenetic relationship of Careae members based on a combined data of the ML and Bayesian analyses. GenBank sequence IDs are given next to species. BS and PP values are given on the branches. Hyphen (-) indicates BS and PP values below than 70% and 0.9, respectively.
FIGURE 1 in Contributions to the taxonomy of the Irano-Turanian genus Rhabdosciadium (Apiaceae): Nomenclatural notes, carpology, molecular phylogeny and the description of a new species from Bitlis (Turkey)
FIGURE 1. Distribution of the Rhabdosciadium species in Turkey: R. hizanense (red), R. anatolyi (blue), R. microcalycinum (purple), R. oligocarpum (grey), and R. urusakii (black).
FIGURE 2 in Contributions to the taxonomy of the Irano-Turanian genus Rhabdosciadium (Apiaceae): Nomenclatural notes, carpology, molecular phylogeny and the description of a new species from Bitlis (Turkey)
FIGURE 2. Distribution of the species Rhabdosciadium in the World: R. hizanense (red), R. anatolyi (blue), R. microcalycinum (purple), R. oligocarpum (grey), R. urusakii (black), R. aucheri (green), R. petiolare (orange), and R. straussii (yellow).
FIGURE 9 in Contributions to the taxonomy of the Irano-Turanian genus Rhabdosciadium (Apiaceae): Nomenclatural notes, carpology, molecular phylogeny and the description of a new species from Bitlis (Turkey)
FIGURE 9. Rhabdosciadium anatolyi in habitat, with Prangos pabularia (from the epitype, M. Fırat 30400).
FIGURE 1 in Debating Liolaemidae diversity and classification, and a bit more: A response to Lobo et al.
FIGURE 1. Phylogenetic topologies of major clades of the Liolaemidae family presented by Schulte et al. (2000, 2004), Espinoza et al. (2004), Cruz et al. (2005) and Abdala (2007), compared to the topology presented in Figure 2 of Pincheira-Donoso et al.'s (2008; abbreviated P-D et al.). Note that all topologies are essentially identical, except of that of Cruz et al., which is in general highly similar in four of the six terminal branches depicted. Also, while Pincheira-Donoso et al.'s topology is entirely identical to Espinoza et al.'s tree, differences with the other four trees are almost entirely explained by different sets of clades included. For example, Ctenoblepharys and Phymaturus were not included in Schulte et al. (2004), while Ctenoblepharys was not included in Schulte et al. (2000). In both cases, however, the only species regarded by Pincheira-Donoso et al. (2008) and Abdala (2007) as member of the anomalus clade that was included in Schulte et al.'s (2000) and Cruz et al.'s (2004) studies, L. pseudoanomalus, is nested within the boulengeri clade. However, as declared by Pincheira-Donoso et al.'s (2008), the anomalus clade was recognized following phylogenetic evidence recently presented by Abdala (2007; see comments number 1 and 7 in the text for additional information). This comparative scheme demonstrates that Lobo et al.'s affirmation that two thirds of the phylogenetic tree presented by Pincheira-Donoso et al. (2008) differ from the rest of known (and cited) phylogenetic hypotheses known for Liolaemidae, is unjustified. Liolaemidae clades are detailed at the right hand side of the panel, where colours that identify lineages are shown. All groups identified as "clades" are lineages of the Liolaemus genus. The archeforuslineomaculatus clade is abbreviated (arch-lineo clade). The name 'boulengeri' clade is the same used by Etheridge (1995) and Espinoza et al. (2004).
BITS-2 Dataset for Fall Detection
<p>Data was collected using a custom-built wrist-worn end worn on the left wrist. Qualcomm Snapdragon 820c. We used MAX30102 Heart rate and SP02 sensor, MPU6500, which gives 3-axis acceleration, 3-axis linear acceleration and 3-axis gyroscope data and GY273 Magnetometer chip for data collection. All the sensors are interfaced to the SoC via the I2C interface using a Mezzanine board.</p><p>Table, each table having six columns, time-stamp, x-axis data, y-axis data and z-axis data, number of axes and type of sensor(label) except in case of heart-rate where there will be only three columns, time-stamp, beats per minute and label (hrt for heart-rate)</p><p>In this data set, the data was collected from a total of 41 volunteers performing 16 ADLs and 8 Falls. Every activity was repeated for five trials.</p>
Chipped and Polished Adze Bit. XCB-105-1989
Chipped and Polished Adze Bit. XCB-105-1989. 400 BCE-100 CE XCB-105 Adamagan (Aleut for place of walrus hunters) is at the head of Morzhovoi Bay, western Alaska Peninsula. It is a massive village with multiple occupations. When it was occupied 400 BCE-100 CE, it was the largest village in the Arctic with an estimated 1000 people. It also has limited occupations dated 2200-1700 BCE, 1000-600 BCE, and 900-1100 CE. The Western Alaska Peninsula artifacts are presented as a result of the research conducted under grants NSF 9630072, NSF 9814086, NSF 9996372, NSF 9996415, NSF 1139266, NSF 1321411. H. Maschner, Principal Investigator. These artifacts were scanned with either a Faro Edge Arm or a Minolta Vivid 9i. Processed in Geomagic or Polyworks. 2-8 photos were used for texture in Geomagic Wrap. Original digitizing work done at the IVL at Id. St. Univ. Subsequent processing and publication completed at Global Digital Heritage. Source: Objaverse 1.0 / Sketchfab
I-BiT - Evaluation of a Novel Binocular Treatment System (I-BiTTM) in Children With Amblyopia
ClinicalTrials.gov study NCT01702727. IPD Sharing: Not stated. Countries: 1. Publications: 3.
Augmenting Buried in Treasures Workshop (BIT) With In-home Decluttering Practice for Individuals With Hoarding Disorder
ClinicalTrials.gov study NCT02377986. IPD Sharing: Not stated. Countries: 0. Publications: 1.
Nostalgia Bits (NOBITS)
ClinicalTrials.gov study NCT02077153. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Script and data used in: A lot of convergence, a bit of divergence: environment and interspecific interactions shape body color patterns in Lissotriton newts
Open the record for dataset details and reuse information.
Power consumption per bit of short distance wireless transmission
<p>Survey results on radio transmitter power consumption per bit reported in 2012 [1] and 2018 [2], and that of 100GbE as a reference. </p> <p>[1] T. Kawanishi, THz and Photonic Seamless Communications, IEEE/OSA J. Lightwave Technol. 37, 1671-1679 (2019)</p> <p>[2] T. Kawanishi, Optical signal processing for millimeter-wave wireless systems, 2012 IEEE Photonics Society Summer Topical Meeting Series, Seattle, WA, 2012.</p>
Dataset related to Analysis of Decoding Failures of LDPC and MDPC Codes in Out-of-Place Bit Flipping Decoding
<p>This dataset contains both the parity check matrix of the two LDPC codes employed in the experimental section of the paper Analysis of Decoding Failures of LDPC and MDPC Codes in Out-of-Place Bit Flipping Decoding, and the delta connected sets found.</p>
BIT List W-European Countries 1959-1989
<p>This is a course trial. The dataset contains all BITs negotiated by West-Germany, Switzerland, France, The Netherlands and the BLEU during the period 1959-1989, as well as selected provisions (FET, FPS, Expropriation, Umbrella clause, Arbitrary and/or discriminatory measures)</p>
FIGURE 7 in Contributions to the taxonomy of the Irano-Turanian genus Rhabdosciadium (Apiaceae): Nomenclatural notes, carpology, molecular phylogeny and the description of a new species from Bitlis (Turkey)
FIGURE 7. Umbel of Rhabdosciadium hizanense (from the holotype, M. Fırat 32618).
FIGURE 6 in Contributions to the taxonomy of the Irano-Turanian genus Rhabdosciadium (Apiaceae): Nomenclatural notes, carpology, molecular phylogeny and the description of a new species from Bitlis (Turkey)
FIGURE 6. Caudex of Rhabdosciadium hizanense (from the holotype, M. Fırat 32618).
FIGURE 5 in Contributions to the taxonomy of the Irano-Turanian genus Rhabdosciadium (Apiaceae): Nomenclatural notes, carpology, molecular phylogeny and the description of a new species from Bitlis (Turkey)
FIGURE 5. Habit of Rhabdosciadium hizanense (from the holotype, M. Fırat 32618).
FIGURE 4 in Contributions to the taxonomy of the Irano-Turanian genus Rhabdosciadium (Apiaceae): Nomenclatural notes, carpology, molecular phylogeny and the description of a new species from Bitlis (Turkey)
FIGURE 4. Rhabdosciadium hizanense in habitat (from the holotype, M. Fırat 32618).
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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)
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DANDI Archive for NWB datasets
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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.