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1,896 results for “call”
Dataset: Global X Nasdaq 100 Covered Call & Growth ETF (QYLG) Stock Performance
This dataset provides historical stock market performance data for specific companies. It enables users to analyze and understand the past trends and fluctuations in stock prices over time. This information can be utilized for various purposes such as investment analysis, financial research, and market trend forecasting.
Dataset: Global X NASDAQ 100 ESG Covered Call ETF (QYLE) Stock Performance
This dataset provides historical stock market performance data for specific companies. It enables users to analyze and understand the past trends and fluctuations in stock prices over time. This information can be utilized for various purposes such as investment analysis, financial research, and market trend forecasting.
Dataset: Global X NASDAQ 100 Covered Call ETF (QYLD) Stock Performance
This dataset provides historical stock market performance data for specific companies. It enables users to analyze and understand the past trends and fluctuations in stock prices over time. This information can be utilized for various purposes such as investment analysis, financial research, and market trend forecasting.
Figures 4-5. 4 in The fast-calling short-tailed cricket Anurogryllus celerinictus Walker, 1973 (Orthoptera: Gryllidae) occurs in Cuba, Greater Antilles
Figures 4-5. 4 Geographical distribution of Anurogryllus celerinictus: previous records (red symbols) and new records (yellow symbols). Image frame = 2,000 x 1,000 km. 5 Habitat and microhabitat of Anurogryllus celerinictus at Havana City, Cuba. This section of the grassy parterre yielded 12 of the examined specimens in three consecutive nights.
Figure 1 in The fast-calling short-tailed cricket Anurogryllus celerinictus Walker, 1973 (Orthoptera: Gryllidae) occurs in Cuba, Greater Antilles
Figure 1. Live Anurogryllus celerinictus from Cuba, photographed in captivity on white background: a) adult male; b– c) same adult female, d) juvenile. Note "short-winged" male and that same female individual displays either "shortwinged" or "long-winged" condition.
Figure 4 in Bryde's whale calls recorded in the Gulf of Mexico
Figure 4. Box-and-whisker plot of mean-adjusted average call rate for Bryde's whale Be9 calls recorded at the DeSoto Canyon HARP during four light periods. Whiskers represent the lowest and the highest datum still within 1.5 interquartile range of the lower and the upper quartile, respectively, and plus symbols are outliers.
Figure 3 in Bryde's whale calls recorded in the Gulf of Mexico
Figure 3. Number of Bryde's whale Be9 calls (black bars) recorded per week at the DeSoto Canyon HARP between 21 October 2010 and 6 July 2011. Gray shaded area is a period during which there was no recording effort and gray dots represent times when there was less than 100% recording effort during the week (right vertical axis).
Figure 2 in Bryde's whale calls recorded in the Gulf of Mexico
Figure 2. Time series and spectrograms of Bryde's whale calls. (A) Be9 pulses recorded with a sonobuoy on 31 July 2011 (600 point FFT, 98% overlap, Hanning window, band-pass filter 60–130 Hz), (B) Be9 call sequence recorded on the HARP at DeSoto Canyon on 8 June 2011 (1,000 point FFT, 95% overlap, Hanning window, band–pass filter 60–130 Hz), and (C) possible Bryde's whale calls recorded on the HARP at DeSoto Canyon on 24 June 2011 (1,000– point FFT, 95% overlap, Hanning window, band–pass filter 110–180 Hz).
Figure 1 in Bryde's whale calls recorded in the Gulf of Mexico
Figure 1. Area of the Gulf of Mexico surveyed from 28 July until 1 August 2011 during AMAPPS cruise (visual survey effort is shown in thick, solid lines). HARP deployment locations at Main Pass (MP), DeSoto Canyon (DC), and Dry Tortugas (DT) are marked with black squares. Bathymetry contours shown at 200 m, 1,000 m, 2,000 m, and 3,000 m. Rectangle is the approximate area of Bryde's whale sightings and recordings on 31 July 2011.
Рис. 3. «ГуΑки» самцов (1) и птенцов (2): a — I. sinensis; b — гибриΑных птиц 2007 г.; c — гибриΑных птиц 2010 г. Fig. 3. "Beeps" of males (1) and nestlings (2): a — I. sinensis; b — hybrid birds 2007; c — hybrid birds 2010 in Call repertoire of Bitterns Ixobrychus in Russian Far East
Рис. 3. «ГуΑки» самцов (1) и птенцов (2): a — I. sinensis; b — гибриΑных птиц 2007 г.; c — гибриΑных птиц 2010 г. Fig. 3. "Beeps" of males (1) and nestlings (2): a — I. sinensis; b — hybrid birds 2007; c — hybrid birds 2010
Рис. 4. Крики беΑствия самок (1): a — I. sinensis; b — гибриΑной птицы; крики беΑствия самцов (2): a — I. minutes (Wroza 2017); b — I. minutes 2007 г.; сΛётков (3): a — 13-суточных I. sinensis; b — 29-суточных I. sinensis; c — 13-суточных гибриΑных птиц; d — 29-суточных гибриΑных птиц Fig. 4. Distress calls of females (1): a — I. sinensis; b — hybrid bird; distress calls of males (2): a — I. minutes (Wroza 2017); b — I. minutes 2007; fledglings (3): a — 13-day-old I. sinensis; b — 29-day-old I. sinensis; c — 13-day-old hybrid birds; d — 29-day-old hybrid birds in Call repertoire of Bitterns Ixobrychus in Russian Far East
Рис. 4. Крики беΑствия самок (1): a — I. sinensis; b — гибриΑной птицы; крики беΑствия самцов (2): a — I. minutes (Wroza 2017); b — I. minutes 2007 г.; сΛётков (3): a — 13-суточных I. sinensis; b — 29-суточных I. sinensis; c — 13-суточных гибриΑных птиц; d — 29-суточных гибриΑных птиц Fig. 4. Distress calls of females (1): a — I. sinensis; b — hybrid bird; distress calls of males (2): a — I. minutes (Wroza 2017); b — I. minutes 2007; fledglings (3): a — 13-day-old I. sinensis; b — 29-day-old I. sinensis; c — 13-day-old hybrid birds; d — 29-day-old hybrid birds
Рис. 1. Брачные крики и их инΑивиΑуаΛьная изменчивость у разных виΑов воΛчков: a — I. m. minutes (Celmins 2008; Bruggen 2017; Maffezzoli 2021); b — I. m. dubius (Graff 2012; Davison 2020); c — I. m. payesii (Hesse 2009; Archer 2019; Cockcroft 2020); d — I. sinensis (Piot 2021; Raveendran 2021; Jeff 2022); e — I. e. exilis (Graves 2021; Overholtz 2021); f — I. e. peruvianus (Moore 2003; Krabbe 2015; Arias 2020); g — I. eurythmus (Mark 1997; Lastukhin 2015; Wulf 2016) Fig. 1. Mating calls and their individual variability in different bittern species: a — I. m.minutes Celmins 2008; Bruggen 2017; Maffezzoli 2021); b — I. m. dubius (Graff 2012; Davison 2020); c — I. m. payesii (Hesse 2009; Archer 2019; Cockcroft 2020); d — I. sinensis (Piot 2021; Raveendran 2021; Jeff 2022); e — I. e. exilis (Graves 2021; Overholtz 2021); f — I. e. peruvianus (Moore 2003; Krabbe 2015; Arias 2020); g — I. eurythmus (Mark 1997; Lastukhin 2015; Wulf 2016) in Call repertoire of Bitterns Ixobrychus in Russian Far East
Рис. 1. Брачные крики и их инΑивиΑуаΛьная изменчивость у разных виΑов воΛчков: a — I. m. minutes (Celmins 2008; Bruggen 2017; Maffezzoli 2021); b — I. m. dubius (Graff 2012; Davison 2020); c — I. m. payesii (Hesse 2009; Archer 2019; Cockcroft 2020); d — I. sinensis (Piot 2021; Raveendran 2021; Jeff 2022); e — I. e. exilis (Graves 2021; Overholtz 2021); f — I. e. peruvianus (Moore 2003; Krabbe 2015; Arias 2020); g — I. eurythmus (Mark 1997; Lastukhin 2015; Wulf 2016) Fig. 1. Mating calls and their individual variability in different bittern species: a — I. m.minutes Celmins 2008; Bruggen 2017; Maffezzoli 2021); b — I. m. dubius (Graff 2012; Davison 2020); c — I. m. payesii (Hesse 2009; Archer 2019; Cockcroft 2020); d — I. sinensis (Piot 2021; Raveendran 2021; Jeff 2022); e — I. e. exilis (Graves 2021; Overholtz 2021); f — I. e. peruvianus (Moore 2003; Krabbe 2015; Arias 2020); g — I. eurythmus (Mark 1997; Lastukhin 2015; Wulf 2016)
Рис. 6. Контактно-тревожная позывка «перекΛичка» птенцов I. sinensis (a) и гибриΑных птиц (b) Fig. 6. Contact-alarm call "roll call" of I. sinensis nestlings (a) and hybrid birds (b) in Call repertoire of Bitterns Ixobrychus in Russian Far East
Рис. 6. Контактно-тревожная позывка «перекΛичка» птенцов I. sinensis (a) и гибриΑных птиц (b) Fig. 6. Contact-alarm call "roll call" of I. sinensis nestlings (a) and hybrid birds (b)
Рис. 5. Контактно-пищевая позывка «мяуканье» (1) и пищевое «шипение» (2) птенцов: a — I. eurythmus; b — I. sinensis; c — гибриΑных птиц Fig. 5. Contact-food "meow" call (1) and food "hissing" (2) of nestlings: a — I. eurythmus; b — I. sinensis; c — hybrid birds in Call repertoire of Bitterns Ixobrychus in Russian Far East
Рис. 5. Контактно-пищевая позывка «мяуканье» (1) и пищевое «шипение» (2) птенцов: a — I. eurythmus; b — I. sinensis; c — гибриΑных птиц Fig. 5. Contact-food "meow" call (1) and food "hissing" (2) of nestlings: a — I. eurythmus; b — I. sinensis; c — hybrid birds
Fig. 3 in New records, range extension and call description for the stream-breeding frog Hyloscirtus lascinius (Rivero, 1970) in Venezuela
Fig. 3. Habitat of Hyloscirtus lascinius at Campamento Guacharaca, Sierra de Perijá, Zulia state (A). Males calling from a branch; (B) and from a rocky wall; (C) at the edge of the creek in Campamento Guacharaca. Photos: F.J.M. RojasRunjaic.
Fig. 2 in New records, range extension and call description for the stream-breeding frog Hyloscirtus lascinius (Rivero, 1970) in Venezuela
Fig. 2. Distribution of Hyloscirtus lascinius in Venezuela and Colombia. 1: Campamento Guacharaca, Sierra de Perijá, Zulia state, Venezuela. 2: San Luis, Mérida state, Venezuela. 3: Road Santa Cruz de Mora-La Macana, Mérida state, Venezuela. 4: Quebrada Ovalles, Mérida state, Venezuela. 5: Quebrada De La Rana, Mérida state, Venezuela. Yellow triangle: Tabor, Tamá massif, Táchira state, Venezuela (type locality); White pentagon: Chinácota, Norte de Santander department, Colombia (Sánchez 2010); The record of headwaters of Río Táchira, Norte de Santander, Colombia (Ruiz-Carranza et al. 1996) and additional localities between Delicias and Tabor (Rivero 1970) are included in the yellow triangle that indicates the type locality.
Fig. 1 in New records, range extension and call description for the stream-breeding frog Hyloscirtus lascinius (Rivero, 1970) in Venezuela
Fig. 1. Hyloscirtus lascinius from Venezuela. (A) Campamento Guacharaca, Sierra de Perijá, Zulia state; (B) Near La Macana, Mérida state; (C) Quebrada La Rana, Mérida state. Photos: F.J.M. Rojas-Runjaic (A) and C.L. Barrio-Amorós (B and C).
colorSV translocation call sets on COLO829 and HCC1395
<p>Translocation call sets generated by colorSV (v0.1.0) on the COLO829 and HCC1395 cell lines as described in the <a href="https://doi.org/10.1101/2024.07.29.605160">colorSV paper</a>.</p>
Name Size Figure 4.2. Ratio of male to female participants-The Effects of CALL on Vocabulary Learning: A Case of Iranian Intermediate EFL Learners
<p>In the past, vocabulary teaching and learning were often given little priority in second<br> language programs but recently there has been a renewed interest in the nature of vocabulary and its<br> role in learning and teaching. Although most teachers might be aware of the importance of<br> technology, say, computer, rarely teachers use it for teaching vocabulary. Thus, the current study<br> aims at exploring the effects of CALL on vocabulary learning of Iranian EFL Learners. In this<br> study, 40 intermediate EFL learners, both male and female aged from 16 to 18 studying New<br> Interchange, book III, were chosen randomly from a language institute in Tehran. They were divided<br> into two twenty-member groups. The experimental group was given the VTS.S (a computer<br> program for teaching vocabularies), a computerized dictionary and provided with teacher efeedback.<br> The control group received no special software and vocabularies were taught using the<br> conventional ways with the help of a paper dictionary.</p>
Figure 4.1. Distribution of scores for the Nelson test-The Effects of CALL on Vocabulary Learning: A Case of Iranian Intermediate EFL Learners
<p>In the past, vocabulary teaching and learning were often given little priority in second<br> language programs but recently there has been a renewed interest in the nature of vocabulary and its<br> role in learning and teaching. Although most teachers might be aware of the importance of<br> technology, say, computer, rarely teachers use it for teaching vocabulary. Thus, the current study<br> aims at exploring the effects of CALL on vocabulary learning of Iranian EFL Learners. In this<br> study, 40 intermediate EFL learners, both male and female aged from 16 to 18 studying New<br> Interchange, book III, were chosen randomly from a language institute in Tehran. They were divided<br> into two twenty-member groups. The experimental group was given the VTS.S (a computer<br> program for teaching vocabularies), a computerized dictionary and provided with teacher efeedback.<br> The control group received no special software and vocabularies were taught using the<br> conventional ways with the help of a paper dictionary. A vocabulary pre-test based on the tests<br> available in their teacher's guide was given to both groups. The aim of this test was to make sure<br> that the students were not familiar with the words in advance. By pre-test/post-test comparison<br> researchers found learners exposed to VTS.S teacher e-feedback plus the computerized dictionary<br> scored higher than the control group. Both high-stake and low-stake holders can avail from the<br> findings of the study.</p>
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.