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794 results for “publishing”
C19 Rapid Reviewers Collaboration - Publisher DataSet for COVID-19 Papers Submitted Jan 2020-March 2021
<p>A dataset from some of the publishers involved in the C19Rapid Reviewer Collaboration. The data shows volumes of submissions and time to publication for COVID-19 papers from specific journals taking part in the initiative from January 2020 until March 2021. The data was supplied by eLife, The Royal Society, Hindawi, GigaScience and CUP.</p>
CAT, TD, ADCP data for CAT research paper to be published in Journal of Water Resource Research
<p>This file contain experiment data obtained in Huangcai reservoir, Hunan, China in September, 2020. The field experiment aimed to reconstruct multi-layer current field using three-dimensional inversion technique to visualize spatiotemporal current structure.</p>
Fig. S1. Temporal evolution of bryophyte UV research. The accumulated number of papers published on the subject is shown.
<p>Temporal evolution of bryophyte UV research.</p>
Supplementary Materials for the article on 'A typology of northwestern Bantu gender systems', published in Linguistics
<p>Scripts, data and figures; documentation is provided</p>
Supplementary Material for 'A typology of northwestern Bantu gender systems', published in Linguistics
<p>documentation is provided in the materials</p>
Dataset for Predatory publishing practices in the shadow of open access models [diploma thesis]
<p>Dataset contains: </p> <ul> <li>a list of predatory journals with ISSNs/eISSNs based upon existing blacklists</li> <li>exports of OA publications from the systems OBD (Charles University personal bibliography database) and RIV (Register of information about research results of the Czech Republic) </li> <li>an analysis based on the data above</li> <li>answers gathered using a quantitative questionnaire on the title topic</li> </ul>
FIGURE 1. Plate 38 in The Callitriche (Plantaginaceae: Callitricheae) names published under the genus Stellaria, and notes on C. aquatica and the Linnéan name C. palustris var. bifida
FIGURE 1. Plate 38 in Loesel (1703), the lectotype of the name Callitriche palustris var. bifida.
Trends in authorship demographics for manuscripts published in Endocrine journals: A 70-year analysis
<p><em><span>Background</span> </em></p> <p><span>Over the previous few decades, demographics, gender, and the amount of papers published have all changed considerably. One of the fields of medicine that has yet to be extensively investigated is endocrinology.</span> </p> <p><em><span>Material and Methods</span> </em></p> <p><span>Journal of Endocrinology and General & Comparative Endocrinology are two landmark journals that publish articles from around the world. We examined each decade during the 70-year period from 1961 to 2021. Funding source, first author – last author gender, their demographics and proportion of papers with at least one female author were the parameters considered while studying each publication. We predicted that the number of female authors per paper would increase with time, as would the range of degrees held by the authors, demographical variations in authorship, and the funding source. Our goal was also to determine the distribution of female first authors and senior authors in endocrinology journals over a 70-year period, as well as to check the gender combinations using the Punnett square. </span> </p> <p><em><span>Results</span> </em></p> <p><span>Female initial authors rose from 7% to 29.6% (p<0.0006) between 1961 and 2021, whereas female senior authors rose from 15.6% to 22.2%. Despite women's small contributions to first and senior authors, female participation rose from 17.48% (25/143) to 70% (170/250) between 1961 and 2021. Male-Female and Female-Male combinations rose with Chi-Square = 124.6, (p<0.0001). Europe and the Americas had the most female academic medical contributors (p<0.0001) Regardless of author status, female participation rose from 17.48% in 1961 to 68% in 2021.</span> </p> <p><em><span>Conclusion </span> </em></p> <p><span>In papers published in endocrinology journals, there was a rising trend in female contributions to academic medicine. Even with the large growth of female endocrinologists, there is still a disparity in why the increase in female authors is comparably fewer.</span> </p>
Solar cell record device efficiency vs number of cumulative publications since first device published
<p>Solar cell record device efficiency either taken from NREL data, or from the authors publication.</p> <p>Cumulative publications are from the Web of Science after 1974, Scopus for after 1959, and Google scholar before.</p>
101! MODELS PUBLISHED
I reached one hundrered models on sketchfab! ENOY WITH ME! Source: Objaverse 1.0 / Sketchfab
Supplementary material 1 from: Vyshedskiy A, Mahapatra S, Dunn R (2017) Linguistically deprived children: meta-analysis of published research underlines the importance of early syntactic language use for normal brain development. Research Ideas and Outcomes 3: e20696. https://doi.org/10.3897/rio.3.e20696
Linguistic isolates performance in verbal and nonverbal tests
Figure 5 from: Vyshedskiy A, Mahapatra S, Dunn R (2017) Linguistically deprived children: meta-analysis of published research underlines the importance of early syntactic language use for normal brain development. Research Ideas and Outcomes 3: e20696. https://doi.org/10.3897/rio.3.e20696
Figure 5 - Flexible syntax, prepositions, adjectives, verb tenses, and other common elements of grammar, all facilitate the human ability to communicate an infinite number of novel images with the use of a finite number of words. The graph shows the number of distinct images that can be transmitted with high fidelity in a communication system with 1,000 nouns as a function of the number of spatial prepositions. In a communication system with no spatial prepositions and other recursive elements, 1000 nouns can communicate 1000 images to a listener. Adding just one spatial preposition allows for the formation of three-word phrases (such as: 'a bowl behind a cup' or 'a cup behind a bowl') and increases the number of distinct images that can be communicated to a listener from 1000 to one million (1000x1x1000). Adding a second spatial preposition and allowing for five-word sentences of the form object-preposition-object-preposition-object (such as: a bowl on a cup behind a plate) increases the number of distinct images that can be communicated to four billion (1000x2x1000x2x1000). The addition of a third spatial preposition increases the number of distinct images to 27 trillion (1000x3x1000x3x1000x3x1000), and so on. In general, the number of distinct images communicated by three-word sentences of the structure object-preposition-object equals the number of object-words times the number of prepositions times the number of object-words. A typical language with 1000 nouns and 100 spatial prepositions can theoretically communicate 1000101 x 100100 distinct images. This number is significantly greater than the total number of atoms in the universe. For all practical purposes, an infinite number of distinct images can be communicated by a syntactic communication system with just 1000 words and a few prepositions. Prepositions, adjectives, and verb tenses dramatically facilitate the capacity of a syntactic communication system with a finite number of words to communicate an infinite number of distinct images. Linguists refer to this property of human languages as recursion. The "infiniteness" of human language has been explicitly recognized by "Galileo, Descartes, and the 17th-century 'philosophical grammarians' and their successors, notably von Humboldt" (Hauser et al. 2002). The infiniteness of all human languages stand in stark contrast to finite homesign communication systems that are lacking spatial prepositions, syntax, and other recursive elements of a formal sign language.
Figure 4 from: Vyshedskiy A, Mahapatra S, Dunn R (2017) Linguistically deprived children: meta-analysis of published research underlines the importance of early syntactic language use for normal brain development. Research Ideas and Outcomes 3: e20696. https://doi.org/10.3897/rio.3.e20696
Figure 4 - Synchronicity has to be understood in terms of synchronicity of the arrival of action potentials to a target neuron rather than absolute equality of action potential conduction times over different paths. Consider the following example: suppose neuron A is receiving excitatory input from neurons B and C via two different pathways (neuron A is the target neuron for both neurons B and C). Suppose that the action potential conduction time is 2ms from neuron B to neuron A and 22ms from neuron C to neuron A (i.e., the axonal pathway B-A has a significantly shorter conduction time than the axonal pathway C-A). Does it mean that the connections B-A and C-A are always asynchronous? No. The answer depends on the predominant neural activity rhythm in this network. At the firing rate of 50Hz (inter-spike interval of 20ms that correspond to Gamma rhythm), neurons B and C can actually be considered synchronous in relationship to neuron A: consider a train of action potentials synchronously fired by neurons B and C. The first action potential from neuron B will reach neuron A in 2ms and the first action potential from neuron C will reach neuron A in 22ms. Obviously, there would be no coincidence in the arrival times of the 1st action potentials from neurons B and C. However the second action potential from neuron B will arrive to neuron A in 22ms, concurrently with the 1st action potential from neuron C. Thus, starting with the second action potential, neuron A will receive synchronous activation from neurons B and C. The synchronous activation has a significantly greater probability of enhancing synaptic connections between neurons A and B, and A and C (Hebbian learning: 'neurons that fire together, wire together' (Hebb 1949). Thus, synchronicity does not need to imply absolute equality in the conduction time over different pathways. Rather synchronicity implies near-zero phase-shift between the two firing trains of action potentials at the postsynaptic cells. This phase-shift depends on conduction times over each pathway and also on the dominant firing frequency in the neural network.
Figure 2 from: Vyshedskiy A, Mahapatra S, Dunn R (2017) Linguistically deprived children: meta-analysis of published research underlines the importance of early syntactic language use for normal brain development. Research Ideas and Outcomes 3: e20696. https://doi.org/10.3897/rio.3.e20696
Figure 2 - A typical question testing subject's ability to mentally rotate an object is shown here as a 2x2 matrix with six answer choices displayed below the problem. The top row of the matrix indicates the rule: "the object in the right column is the result of 45° clockwise rotation." Applying this rule to the bottom row, we arrive at the correct answer depicted on the right.
Figure 1 from: Vyshedskiy A, Mahapatra S, Dunn R (2017) Linguistically deprived children: meta-analysis of published research underlines the importance of early syntactic language use for normal brain development. Research Ideas and Outcomes 3: e20696. https://doi.org/10.3897/rio.3.e20696
Figure 1 - Visual information processing in the cortex. From the primary visual cortex (V1, shown in yellow), the visual information is passed in two streams. The neurons along the ventral stream also known as the ventral visual cortex (shown in purple) are primarily concerned with what the object is. The ventral visual stream runs into the inferior temporal lobe. The neurons along the dorsal stream also known the dorsal visual cortex (shown in green) are primarily concerned with where the object is. The dorsal visual stream runs into the parietal lobe.
Figure 3 from: Vyshedskiy A, Mahapatra S, Dunn R (2017) Linguistically deprived children: meta-analysis of published research underlines the importance of early syntactic language use for normal brain development. Research Ideas and Outcomes 3: e20696. https://doi.org/10.3897/rio.3.e20696
Figure 3 - Linguistic isolates performance in verbal and nonverbal tests. This Figure is also available as a Power Point slide in Suppl. material 1.
Figure 6 from: Penev L, Mietchen D, Chavan V, Hagedorn G, Smith V, Shotton D, Ó Tuama É, Senderov V, Georgiev T, Stoev P, Groom Q, Remsen D, Edmunds S (2017) Strategies and guidelines for scholarly publishing of biodiversity data. Research Ideas and Outcomes 3: e12431. https://doi.org/10.3897/rio.3.e12431
Figure 6 - Automated creation of data paper manuscripts from Ecological Metadata Language (EML) metadata in the ARPHA Writing Tool.
Figure 5 from: Penev L, Mietchen D, Chavan V, Hagedorn G, Smith V, Shotton D, Ó Tuama É, Senderov V, Georgiev T, Stoev P, Groom Q, Remsen D, Edmunds S (2017) Strategies and guidelines for scholarly publishing of biodiversity data. Research Ideas and Outcomes 3: e12431. https://doi.org/10.3897/rio.3.e12431
Figure 5 - The metadata from the GBIF Integrated Publishing Toolkit (IPT) can be downloaded as RTF or EML files and submitted to Pensoft's journals as data paper manuscripts.
Figure 3 from: Penev L, Mietchen D, Chavan V, Hagedorn G, Smith V, Shotton D, Ó Tuama É, Senderov V, Georgiev T, Stoev P, Groom Q, Remsen D, Edmunds S (2017) Strategies and guidelines for scholarly publishing of biodiversity data. Research Ideas and Outcomes 3: e12431. https://doi.org/10.3897/rio.3.e12431
Figure 3 - The user interface of the ARPHA Writing Tool through which single or multiple specimen records from GBIF, BOLD, iDigBio and PlutoF are imported through records identifiers.
Figure 1 from: Penev L, Mietchen D, Chavan V, Hagedorn G, Smith V, Shotton D, Ó Tuama É, Senderov V, Georgiev T, Stoev P, Groom Q, Remsen D, Edmunds S (2017) Strategies and guidelines for scholarly publishing of biodiversity data. Research Ideas and Outcomes 3: e12431. https://doi.org/10.3897/rio.3.e12431
Figure 1 - Recommendation of Dryad to cite both the original article in association with which the data were published and the data themselves.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.