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2,837 results for “Climate Data”
Data for the manuscript: Planning for climate migration in Great Lake Legacy Cities
<p>Our analysis for the manuscript, "Planning for climate migration in Great Lake Legacy Cities" uses county level spatial data from the FEMA National Risk Index (USFEMA, 2021) and the CDC SVI ranking system (ATSDR, 2018) in the form of shapefiles(.shp). To create the geovisualization, we used boundaries of the Great Lakes that are published here https://www.glc.org/greatlakesgis. All analysis was conducted using R (2020), with code that can be found here: https://derekvanberkel.github.io/Planning-for-climate-migration-in-Great-Lake-Legacy-Cities/ </p> <p>ATSDR. (2018). Cdc/atsdr social vulnerability index. https://www.atsdr.cdc.gov/placeandhealth/svi/fact sheet/fact sheet.html.</p> <p>USGCRP. (2018). Impacts, risks, and adaptation in the united states: Fourth national climate assessment. US Global Change Research Program.</p> <p> </p>
Data from: A novel laboratory method to simulate climatic stress with successful application to experiments with medically relevant ticks
<p>Ticks are the most important vectors of zoonotic disease-causing pathogens in North America and Europe. Many tick species are expanding their geographic range. Although correlational evidence suggests that climate change is driving the range expansion of ticks, experimental evidence is necessary to develop a mechanistic understanding of ticks' response to a range of climatic conditions. Previous experiments used simulated microclimates, but these protocols require hazardous salts or expensive laboratory equipment to manipulate humidity. We developed a novel, safe, stable, convenient, and economical method to isolate individual ticks and manipulate their microclimates. The protocol involves placing individual ticks in plastic tubes, and placing six tubes along with a commercial two-way humidity control pack in an airtight container. We successfully used this method to investigate how humidity affects survival and host-seeking (questing) behavior of three tick species: the lone star tick (Amblyomma americanum), American dog tick (Dermacentor variabilis), and black-legged tick (Ixodes scapularis). We placed 72 adult females of each species individually into plastic tubes and separated them into three experimental relative humidity (RH) treatments representing distinct climates: 32% RH, 58% RH, and 84% RH. We assessed the survival and questing behavior of each tick for 30 days. In all three species, survivorship significantly declined in drier conditions. Questing height was negatively associated with RH in Amblyomma, positively associated with RH in Dermacentor, and not associated with RH in Ixodes. The frequency of questing behavior increased significantly with drier conditions for Dermacentor but not for Amblyomma or Ixodes. This report demonstrates an effective method for assessing the viability and host-seeking behavior of tick vectors of zoonotic diseases under different climatic conditions.</p>
Data for Contrasting life-history responses to climate variability in eastern and western North Pacific sardine populations
<p><span>Massive populations of sardines inhabit both the western and eastern boundaries of the world's subtropical ocean basins, supporting both commercial fisheries and populations of marine predators. Sardine populations in western and eastern boundary current systems have responded oppositely to decadal scale anomalies in ocean temperature, but the mechanism for differing variability has remained unclear. Here, based on otolith microstructure and high-resolution stable isotope analyses, we show that habitat temperature, early life growth rates, energy expenditure, metabolically optimal temperature and, most importantly, the relationship between growth rate and temperature were remarkably different between the two subpopulations in the western and eastern North Pacific. Varying metabolic response to environmental changes partly explain the contrasting growth responses. Consistent differences in the life-history traits are observed between subpopulations in the western and eastern boundary current systems around South Africa. These growth and survival characteristics can facilitate the contrasting responses of sardine populations to climate change.</span></p>
Model output data for Smith et al., "Effects of increasing the category resolution of the sea ice thickness distribution in a coupled climate model on Arctic and Antarctic sea ice"
<p>Model output data for Smith et al., "Effects of increasing the category resolution of the sea ice thickness distribution in a coupled climate model on Arctic and Antarctic sea ice", in review in Journal of Geophysical Research-Oceans, 2022. Details on CESM model settings and run setups can be found within the manuscript. </p>
Data from: The evolution of sex similarities in social signals: Climatic seasonality is associated with lower sexual dimorphism and greater elaboration of female and male signals in antbirds (Thamnophilidae)
<p>Selection on signals that mediate social competition varies with resource availability. Climate regulates resource availability, which may affect the strength of competition and selection on signals. Traditionally, this meant that more seasonal, colder, or dryer – overall harsher – environments should favor the elaboration of male signals under stronger male-male competition, increasing sexual dimorphism. However, females also use signals to compete; thus, harsher environments could strengthen competition and favor elaboration of signals in both sexes, decreasing sexual dimorphism. Alternatively, harsher environments could decrease sexual dimorphism due to scarcer resources to invest in signal elaboration in both sexes. We evaluated these contrasting hypotheses in antbirds, a family of Neotropical passerines that varies in female and male signals and occurs across diverse climatic regimes. We tested the association of sexual dimorphism of plumage coloration and songs with temperature, precipitation and their seasonality. We found that greater seasonality is associated with lower sexual dimorphism in plumage coloration and greater elaboration of visual signals in both sexes, but not acoustic signals. Our results suggest that greater seasonality may be associated with convergent elaboration of female and male visual signals, highlighting the role of signals of both sexes in the evolution of sexual dimorphism.</p>
CRAAS: Cloud Regime dAtAset based on the CLAAS-2.1 climate data record
<p>The Cloud Regime dAtAset based on the CLAAS-2.1 climate data record (CRAAS) is a dataset of cloud regimes derived from cloud properties from the <a href="https://wui.cmsaf.eu/safira/action/viewDoiDetails?acronym=CLAAS_V002_01">CLAAS-2.1</a> climate data record. Such a cloud regime dataset can provide detailed insight in the cloud climatology over the region of interest and also in climate monitoring through the concept of the cloud regimes.</p> <p>CRAAS covers a region over Europe (30°N to 60°N and from 11°W to 37°E) and it extends from 2004 to 2017. The generated Joint Cloud Histograms (JCHs) of Cloud Top Pressure (CTP) and Cloud Optical Thickness (COT), <br> as well as the derived labeled data points of the cloud regime classification are available on a 1°x1° degree resolution and every 15 minutes.</p> <p>Two sets of yearly files can be found in the dataset. Those containing the generated JCHs from the CLAAS-2.1 climate data record (example filename: 'craas_jch_2004.v1.nc') <br> and those including the labeled data points of the cloud regime classification (example filename: 'craas_label_2004.v1.nc').<br> The files are provided in netCDF4 format, following the NetCDF Climate and Forecast Metadata Conventions-Version 1.8 (CF-1.8).</p>
Data and code – Effects of climate on salmonid productivity: A global meta-analysis across freshwater ecosystems
<p>Salmonids are of immense socio-economic importance in much of the world but are threatened by climate change. This has generated a substantial literature documenting effects of climate variation on salmonid productivity in freshwater ecosystems, but there has been no global quantitative synthesis across studies. We conducted a systematic review and meta-analysis to gain quantitative insight into key factors shaping the effects of climate on salmonid productivity, ultimately collecting 1,321 correlations from 156 studies, representing 23 species across 24 countries. Fisher's Z was used as the standardized effect size, and a series of weighted mixed-effects models were compared to identify covariates that best explained variation in effects. Patterns in climate effects were complex, and were driven by spatial (latitude, elevation), temporal (time-period, age-class), and biological (range, habitat type, anadromy) variation within and among study populations. These trends were often consistent with predictions based on salmonid thermal tolerances. Namely, warming and decreased precipitation tended to reduce productivity when high temperatures challenged upper thermal limits, while opposite patterns were common when cold temperatures limited productivity. Overall, variable climate impacts on salmonids suggest that future declines in some locations may be counterbalanced by gains in others. In particular, we suggest that future warming should (1) increase salmonid productivity at high latitudes and elevations (especially >60° and >1,500m), (2) reduce productivity in populations experiencing hotter and dryer growing season conditions, (3) favor non-native over native salmonids, and (4) impact lentic populations less negatively than lotic ones. These patterns should help conservation and management organizations identify populations most vulnerable to climate change, which can then be prioritized for protective measures. Our framework enables broad inferences about future productivity that can inform decision-making under climate change for salmonids and other taxa, but more widespread, standardized, and hypothesis-driven research is needed to expand current knowledge.</p>
Data from: Can extreme climatic events induce shifts in adaptive potential? A conceptual framework and empirical test with Anolis lizards
<p>Multivariate adaptation to climatic shifts may be limited by trait integration that causes genetic variation to be low in the direction of selection. However, strong episodes of selection induced by extreme climatic pressures may facilitate future population-wide responses if selection reduces trait integration and increases adaptive potential (i.e., evolvability). We explain this counter-intuitive framework for extreme climatic events in which directional selection leads to increased evolvability and exemplify its use in a case study. We tested this hypothesis in two populations of the lizard <em>Anolis scriptus</em> that experienced hurricane-induced selection on limb traits. We surveyed populations immediately before and after the hurricane as well as the offspring of post-hurricane survivors, allowing us to estimate both selection and response to selection on key functional traits: forelimb length, hindlimb length, and toepad area. Direct selection was parallel in both islands and strong in several limb traits. Even though overall limb integration did not change after the hurricane, both populations showed a non-significant tendency toward increased evolvability after the hurricane despite the direction of selection not being aligned with the axis of most variance (i.e., body size). The population with comparably lower between-limb integration showed a less constrained response to selection. Hurricane-induced selection, not aligned with the pattern of high trait correlations, likely conflicts with selection occurring during normal ecological conditions that favor functional coordination between limb traits, and would likely need to be very strong and more persistent to elicit a greater change in trait integration and evolvability. Future tests of this hypothesis should use G-matrices in a variety of wild organisms experiencing selection due to extreme climatic events. </p>
Code and data used in "A Tool for Air Pollution Scenarios (TAPS v1.0) to enable global, long-term, and flexible study of climate and air quality policies"
<p>Data and code for Tool for Air Pollution Scenarios (TAPS v1.0) as submitted to Geoscientific Model Development for publication. See the enclosed README and full user manual (https://github.com/watkin-mit/TAPS/wiki) for more information. </p>
Supplementary material 1 from: Motloung R, Robertson M, Rouget M, Wilson J (2014) Forestry trial data can be used to evaluate climate-based species distribution models in predicting tree invasions. NeoBiota 20: 31-48. https://doi.org/10.3897/neobiota.20.5778
Current and potential distributions of sixteen species that are not widespread in southern Africa arranged on the basis of their suitable range size : a) Acacia paradoxa, b) A. cultriformis, c) A. falciformis, d) A. pendula, e) A. rubida, f) A. stricta, g) A. retinodes, h) A. fimbriata, i) A. aneura, j) A. viscidula, k) A. acuminata, l) A. adunca, m) A. binervata, n) A. schinoides, o) A. prominens, p) A. mangium. The grey shading indicates areas that SDMs have identified as suitable by SDMs while the white ones are unsuitable.
Data and scripts for figures in Walton & Huntingford, "Little Evidence of Hysteresis in Regional Precipitation, When Indexed by Global Temperature Rise and Fall in an Overshoot Climate Simulation"
<p>The datasets included here are of the plotted data from the figures of the paper entitled "Little Evidence of Hysteresis in Regional Precipitation, When Indexed by Global Temperature Rise and Fall in an Overshoot Climate Simulation", submitted for publication to Environmental Research Letters. Scripts used for plotting and analysis are also included.</p>
Synthetic Indoor Climate and Occupancy Data from Office and Meeting Room Simulations
<p>This is the dataset used for the publication "Coddora: CO2-based Occupancy Detection model<br>trained via DOmain RAndomization". The goal is to provide training data for occupancy detection.<br><br>The dataset contains one million days of data including 10 occupied days for each of 100,000 randomized room models (50,000 rooms considering office activity and 50,000 meeting room activity). Data were generated in EnergyPlus simulations according to the methodology described in the paper.<br><br>When using the dataset, please cite:</p> <blockquote> <p><em>Manuel Weber, Farzan Banihashemi, Davor Stjelja, Peter Mandl, Ruben Mayer, and Hans-Arno Jacobsen. 2024. Coddora: CO2-Based Occupancy Detection Model Trained via Domain Randomization. In International Joint Conference on Neural Networks (IJCNN). June 30 - July 5, 2024, Yokohama, Japan.</em></p> </blockquote> <h2>Dataset Structure</h2> <p>The following files are provided:<br><br> 1. dataset_office_rooms.h5 (provided as zip file)<br> 2. dataset_meeting_rooms.h5 (provided as zip file)<br> 3. simulated_occupancy_office_rooms.csv<br> 4. simulated_occupancy_meeting_rooms.csv</p> <p>Please use an archiving tool such as 7zip to unzip the hdf5 files.<br>Both hdf5 files contain two datasets with the following keys:<br><br> 1. "<em>data</em>": contains the simulated indoor climate and occupancy data<br> 2. "metadata": contains the metadata that were used for each simulation</p> <p>The csv files contain the time series of occupancy that were used for the simulations.<br><br></p> <h2>Data</h2> <p><em>Data</em> includes the following fields:</p> <p><em>Datetime:</em> day of the year (may be relevant due to seasonal differences) and time of the day<br><em>Zone Air CO2 Concentration:</em> CO2 level in ppm<br><em>Zone Mean Air Temperature:</em> temperature in °C<br><em>Zone Air Relative Humidity: </em>relative humidity in %<br><em>Occupancy: </em>level of occupancy relative to the maximum capacity of the room (in the range [0-1])<br><em>Ventilation:</em> fraction of window opening in the range [0.01, 1]<br><em>SimID:</em> foreign key to reference the room properties the simulation was based on<br><em>BinaryOccupancy:</em> 0 or 1 denoting absence or presence (for binary classification)</p> <p> </p> <p>Example row:</p> <table> <tbody> <tr> <th><em>Datetime</em></th> <th><em>Zone Air CO2 Concentration</em></th> <th><em>Zone Mean Air Temperature</em></th> <th><em>Zone Air Relative Humidity</em></th> <th><em>Occupancy</em></th> <th><em>Ventilation</em></th> <th><em>simID</em></th> <th><em>BinaryOccupancy</em></th> </tr> <tr> <td> <p>10/09 11:21:00</p> </td> <td> <p>1084.5624647371608</p> </td> <td> <p>24.545635909907148</p> </td> <td> <p>41.18393114737054</p> </td> <td> <p>0.7</p> </td> <td> <p>0.0</p> </td> <td>99</td> <td>1</td> </tr> </tbody> </table> <pre> </pre> <h2>Metadata</h2> <p><em>Metadata</em> includes the following fields. <br>Underscores denote that the field was not selected during randomization but calculated from the other values.</p> <p>width: room width in m<br>length: room length in m<br>height: hoom height in m<br>infiltration: infiltration per exterior area in m³/m²s<br>outdoor_co2: co2 concentration in the outdoor air in ppm (set to a random value between [300, 500])<br>orientation: angle between the room's facade orientation and the north direction in degrees<br>maxOccupants: room occupation limit, i.e. the maximum number of occupants<br>_floorArea: floor area in m² (calculated from room dimensions)<br>_volume: room volume in m³ (calculated from room dimensions)<br>_exteriorSurfaceArea: surface area of the facade wall (calculated from room dimensions)<br>_winToFloorRatio: ratio between total window area and floor area (calculated from room model)<br>firstDayUsedOfOccupancySequence: selected starting day in the sequence of occupancy data for rooms with the respective maxOccupants value<br>simID: unique identifier of the simulation to relate between simulation metadata and resulting simulated data</p> <p> </p> <p>Example row:</p> <table> <tbody> <tr> <th>width</th> <th>length</th> <th>height</th> <th>infiltration</th> <th>outdoor_co2</th> <th>orientation</th> <th>maxOccupants</th> <th>_floorArea</th> <th>_volume</th> <th>_exteriorSurfaceArea</th> <th>_winToFloorRatio</th> <th>firstDayOfUsedOccupancySequence</th> <th>simID</th> </tr> <tr> <td>5.481</td> <td>5.190</td> <td>3.264</td> <td>0.000214</td> <td>438.0</td> <td>316.0</td> <td>4.0</td> <td>28.446</td> <td>92.849</td> <td>16.940</td> <td>0.216</td> <td>192</td> <td>0</td> </tr> </tbody> </table> <p> </p> <h2>Occupancy Data</h2> <p>The occupancy data provided through the separate csv files contain the data from the upfront occupancy simulations that the climate simulation was based on. For each level of considered room occupancy limit (maxOccupants), the datasets provide minute values of occupancy throughout 1000 days.</p> <p><em>Datetime, </em><em>Date, </em><em>Timestamp: fictive time of simulated occupancy record (sequences are in 1-minute resolution)</em><br><em>Occupants: number of present occupants</em><br><em>Occupancy: binary occupancy state (0=unoccupied, 1=occupied)</em><br><em>WindowState: binary state of ventilation (0=windows closed, 1=room is ventilated)</em><br><em>maxOccupants: maximum number of occupants considered for the simulated sequence</em><br><em>WindowOpeningFraction: fractional extent to which windows are opened, within the interval [0.01, 1]<br><br></em></p> <p>Example row:</p> <table> <tbody> <tr> <th>Datetime</th> <th>Date</th> <th>Timestamp</th> <th>Occupants</th> <th>Occupancy</th> <th>WindowState</th> <th>maxOccupants</th> <th>WindowOpeningFraction</th> </tr> <tr> <td>2023-01-01 00:00:00</td> <td>2023-01-01</td> <td>1.672531e+09</td> <td>0</td> <td>0</td> <td>0</td> <td>1</td> <td>0.0</td> </tr> </tbody> </table> <p> </p> <p> </p>
Data and code for high-resolution climate-resilient corridor mapping in southwestern Costa Rica (beta)
<p>High-resolution mapping and validation of potential climate-resilient corridors in southwestern Costa Rica. A fully documented, complete version of this repository will be archived with a DOI upon manuscript publication.</p>
Data from: Climate change and population persistence in a hibernating marsupial
<p>Climate change has physiological consequences on organisms, ecosystems, and human societies, surpassing the pace of organismal adaptation. Hibernating mammals are particularly vulnerable as winter survival is determined by short-term physiological changes triggered by temperature. In these animals, winter temperatures cannot surpass certain threshold, above which hibernators arouse from torpor, increasing several fold their energy needs when food is unavailable. Here, we parameterized a numerical model predicting energy consumption in heterothermic species, and modeled winter survival at different climate change scenarios. As a model species, we used the arboreal marsupial monito del monte (genus <em>Dromiciops</em>) which is recognized as one of the few South America hibernators. We modeled four climate change scenarios (from optimistic to pessimistic), based on IPCC projections, predicting that northern and coastal populations (<em>Dromiciops bozinovici</em>) will decline because the minimum number of cold days needed to survive the winter will not be attained. These populations are also the most affected by habitat fragmentation and change in land use. Conversely, Andean and other highland populations at cooler environments, are predicted to persist and thrive. Given the widespread presence of hibernating mammals around the world, models based on simple physiological parameters such as this one, are becoming essential for predicting species responses to warming in the short term.</p>
Data from: In situ decrease in rhodolith growth associated with Arctic climate change
<p>Rhodoliths built by crustose coralline algae (CCA) are ecosystem engineers of global importance. In the Arctic photic zone, their three-dimensional growth emulates the habitat complexity of coral reefs but with a far slower growth rate, growing at micrometres per year rather than millimetres. While climate change is known to exert various impacts on the CCA's calcite skeleton, including geochemical and structural alterations, field observations of net growth over decade-long timescales are lacking. Here, we use a temporally-explicit model to show that rising ocean temperatures over nearly 100 years were associated with reduced rhodolith growth at different depths in the Arctic. Over the past 90 years, the median growth rate was 85 µm yr<sup>-1</sup> but each °C increase in summer seawater temperature decreased growth by a mean of 8.9 µm (95% CIs = 1.32 - 16.60 µm °C<sup>-1</sup>, p < 0.05). The decrease was expressed for rhodolith occurrences in 11 and 27 m water depth but not at 46 m, also having the shortest time series (1991 – 2015). Although increasing temperatures can spur plant growth, we suggest anthropogenic climate change has either exceeded the population thermal optimum for these CCA, or synergistic effects of warming, ocean acidification, and/or increasing turbidity impair rhodolith growth. Rhodoliths built by calcitic CCA are important habitat providers worldwide, so decreased growth would lead to yet another facet of anthropogenic habitat loss.</p>
Data from: Climatic disequilibrium of recruit communities across a drought-induced die-off gradient in Mediterranean shrubland
<p>Positive plant–plant interactions (facilitation) may enhance the recruitment and establishment of species less adapted to local macroclimatic conditions. A major cause of this effect is climatic buffering, which implies an increased mismatch between the macroclimatic conditions and the climatic requirements of the existing community – climatic disequilibrium – of plants living under canopies. Here we explore the effect of drought-induced defoliation of Mediterranean shrubland canopy on the recruitment of woody species. We analyzed the differences in the climatic disequilibrium across different categories of canopy defoliation and plant–plant interactions: facilitation, neutral and inhibition. Climatic disequilibrium was estimated as the Euclidean distance in the multivariate environmental space between observed macroclimate and community inferred climate. The inferred climate was calculated by averaging the coordinates of the species' climatic niche centroids, obtained from species distribution, weighted by the species' relative abundances in each community. We found that the recruiting community growing under canopy showed higher climatic disequilibrium than the community growing in the gaps. The facilitated recruiting community growing under dead and living canopy showed the highest disequilibrium, followed by the community growing under mid-affected canopy. The climatic disequilibrium of the recruiting communities experiencing neutral and inhibited interaction was not affected by canopy defoliation. These findings indicate that the climatic disequilibrium of the recruiting community is determined by the facilitation–competition balance. Living canopy provides climatic buffering, but it also implies competition, while dead canopy may provide some structural climatic buffering, without implying competition for resources. These results highlight the relevance of incorporating plant–plant interactions, particularly facilitation, to better forecast plant community responses to extreme climate events and climate change.</p>
Data and original code for: Explaining the diversity of optical effects in Christmas beetles: climate, history, and mechanisms
<p><span>Beetles exhibit an extraordinary diversity of brilliant and colourful appearances. The mechanisms producing these optical effects have received some attention, but we know little about the ecological variables driving their evolution. Here we investigated environmental correlates of reflectivity and circular polarization produced by a combination of pigments and structures in optically diverse Christmas beetles (Scarabaeidae: Rutelinae). We quantified the optical properties of 261 specimens representing 46 species using spectrophotometry and calibrated photographs. Then, we examined associations between these properties and environmental variables such as temperature, humidity, and vegetation cover, controlling for body size and phylogenetic relatedness. Our results showed that larger beetles have higher reflectivity and occur in drier environments. Unexpectedly, near-infrared (NIR) reflectivity was not correlated with ecological variables. We observed no universal ecogeographical pattern for polarization but identified trade-offs with other optical properties: beetles without polarization-associated nanostructures had higher NIR reflectivity. Visible reflectivity seems less affected by nanostructures and is instead negatively correlated with the accumulation of pigments such as melanin. Our study highlights the value of a macroecological approach for testing alternative hypotheses to explain the diversity of optical effects in beetles and to understand the link between structure and function.</span></p>
Figure 6 in Forest yield prediction under different climate change scenarios using data intelligent models in Pakistan
Figure 6. Empirical cumulative distribution function (ECDF) of the Predicted error |PE| (cft) in testing period for the RF and KRR models between the predicted and observed yields of Blue pine and Silver fir species.
Figure 4 in Forest yield prediction under different climate change scenarios using data intelligent models in Pakistan
Figure 4. Box-plots of the Predicted error | PE| (cft) in testing period (1996-2016) for the RF and KRR models between the predicted and observed yields of Blue pine and Silver fir species.
Figure 7 in Forest yield prediction under different climate change scenarios using data intelligent models in Pakistan
Figure 7. Taylor diagram showing the correlation coefficient between the predicted and observed yields (Blue pine and Silver fir) (cft) and standard deviation for the RF and KRR models.
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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.