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Research data keyboard_double_arrow_right Dataset 2023Publisher:Zenodo Authors: Matteo, Nigro; Michele, Barsanti; Roberto, Giannecchini;The version 1.0 contains the supporting data for the work (still under submission) "Last century changes in annual precipitation in a Mediterranean area and their spatial variability. Insights from northern Tuscany (Italy)". The following files are here available (all file are georeferenced in EPSG: 3003): - AVG_Rainfall_1990-2019.tif -> Raster map of the mean annual precipitation for the northern Tuscany, Italy. It encompasses the portion of the Tuscany region northern of the cities of Livorno - Florence. The interpolation was validated via a leave one out cross-validation procedure. - D3-1_Area2_ApuanAlps.tif -> Raster map of the differences in mean annual precipitation between the two 3-decades periods 1921 to 1950 and 1990 to 2019 for the Apuan Alps mountain ridge (Tuscany, Italy). - D3-2_Area2_ApuanAlps.tif -> Raster map of the differences in mean annual precipitation between the two 3-decades periods 1951 to 1980 and 1990 to 2019 for the Apuan Alps mountain ridge (Tuscany, Italy). - DeltaSHP_Points_AVG_Annual_Rainfall.zip -> Shape file of the raingauges locations with the mean annual precipitation values of the period 1990 to 2019. - RaingaugesSHP_Points_AVG_Annual_Rainfall_1990-2019.zip -> Shape file of the raingauges locations with the following information: differences in the mean annual precipitation values between the two 3-decades periods 1951 to 1980 and 1990 to 2019 (named D3-2); p values of the t-test for significance of the differences between the mean annual precipitation ofthe two 3-decades periods 1951 to 1980 and 1990 to 2019; difference in the mean annual precipitation values between the two 3-decades periods 1921 to 1950 and 1990 to 2019 (named D3-1); p values of the t-test for significance of the differences between the mean annual precipitation ofthe two 3-decades periods 1921 to 1950 and 1990 to 2019.
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You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5281/zenodo.7822115&type=result"></script>'); --> </script>
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You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5281/zenodo.7822115&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2016Publisher:Zenodo Authors: Ruest, Nick;Consists of a web crawl of unique URLs tweeted with the #YMMFire hashtag. #YMMFire collection took place from May 1-June 25, 2016. Unique URLs were extracted from the dataset, and harvested with Heritrix on August 31-September 2, 2017. This research was supported by a research grant -- 435-2015-0011 -- issued by Social Sciences and Humanities Research Council.
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You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5281/zenodo.5248247&type=result"></script>'); --> </script>
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You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5281/zenodo.5248247&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2024Embargo end date: 05 Mar 2024Publisher:Dryad Authors: Parra, Adriana; Greenberg, Jonathan;This README file was generated on 2024-03-04 by Adriana Parra. ## GENERAL INFORMATION 1\. Title of Dataset: **Climate-limited vegetation change in the conterminous United States of America** 2\. Author Information A. First Author Contact Information Name: Adriana Parra Institution: University of Nevada, Reno Address: Reno, NV USA Email: adrianaparra@unr.edu B. Co-author Contact Information Name: Jonathan Greenberg Institution: University of Nevada, Reno Address: Reno, NV USA Email: jgreenberg@unr.edu 3\. Coverage period of the dataset: 1986-2018 4\. Geographic location of dataset: Conterminous United States 5\. Description: This dataset contains the input and the resulting rasters for the study “CLIMATE-LIMITED VEGETATION CHANGE IN THE CONTERMINOUS UNITED STATES OF AMERICA”, published in the Global Change Biology journal. The dataset includes a) the observed rates of vegetation change, b) the climate derived potential vegetation rates of change, c) the difference between potential and observed values and d) the identified climatic limiting factor. Additionally, the dataset includes a legend file for the identified climatic limiting factor rasters. ## SHARING/ACCESS INFORMATION 1\. Links to publications that cite or use the data: **Parra, A., & Greenberg, J. (2024). Climate-limited vegetation change in the conterminous United States of America. Global Change Biology, 30, e17204. [https://doi.org/10.1111/gcb.17204](https://doi.org/10.1111/gcb.17204)** 2\. Links to other publicly accessible locations of the data: None 3\. Links/relationships to ancillary data sets: None 4\. Was data derived from another source? Yes A. If yes, list source(s): "Vegetative Lifeform Cover from Landsat SR for CONUS" product publicly available in the ORNL DAAC (https://daac.ornl.gov/cgi-bin/dsviewer.pl?ds_id=1809) TerraClimate data catalog publicly available at the website https://www.climatologylab.org/terraclimate.html 5\. Recommended citation for this dataset: Parra, A., & Greenberg, J. (2024). Climate-limited vegetation change in the conterminous United States of America. Global Change Biology, 30, e17204. [https://doi.org/10.1111/gcb.17204](https://doi.org/10.1111/gcb.17204) ## DATA & FILE OVERVIEW This dataset contains 16 geotiff files, and one csv file. There are 4 geotiff files per each of the lifeform classes evaluated in this study: herbaceous, tree, shrub, and non-vegetation. The files corresponding to each lifeform class are indicated by the first two letters in the file name, HC indicates herbaceous cover, TC indicates tree cover, SC indicates shrub cover, and NC indicates non-vegetation cover. 1\. File List: a) Observed change: Trends of vegetation change between 1986 and 2018. b) Potential predict: Predicted rates of vegetation change form the climate limiting factor analysis. c) Potential observed difference: Difference between the potential and the observed vegetation rates of change. d) Limiting variable: Climate variable identified as the limiting factor for each pixel the conterminous United States. e) Legend of the Limiting variable raster All the geotiff files are stored as Float 32 type, and in CONUS Albers Equal Area coordinate system (EPSG:5070) The csv file included in the dataset is the legend for the limiting variable geotiff files. This file includes the name of the climate variable corresponding to each number in the limiting variable files, as well as information on the variable type and the corresponding time lag. 2\. Relationship between files, if important: None 3\. Additional related data collected that was not included in the current data package: None 4\. Are there multiple versions of the dataset? No A. If yes, name of file(s) that was updated: NA i. Why was the file updated? NA ii. When was the file updated? NA Input data We use the available data from the “Vegetative Lifeform Cover from Landsat SR for CONUS” product (https://daac.ornl.gov/cgi-bin/dsviewer.pl?ds_id=1809) to evaluate the changes in vegetation fractional cover. The information for the climate factors was derived from the TerraClimate data catalog (https://www.climatologylab.org/terraclimate.html). We downloaded data from this catalog for the period 1971 to 2018 for the following variables: minimum temperature (TMIN), precipitation (PPT), actual evapotranspiration (AET), potential evapotranspiration (PET), and climatic water deficit (DEF). Preprocessing of vegetation fractional cover data We resampled and aligned the maps of fractional cover using pixel averaging to the extent and resolution of the TerraClimate dataset (~ 4 km). Then, we calculated rates of lifeform cover change per pixel using the Theil-Sen slope analysis (Sen, 1968; Theil, 1992). Preprocessing of climate variables data To process the climate data, we defined a year time step as the months from July of one year to July of the next. Following this definition, we constructed annual maps of each climate variable for the years 1971 to 2018. The annual maps of each climate variable were further summarized per pixel, into mean and slope (calculated as the Theil-Sen slope) across one, two, three, four, five, ten-, and 15-year lags. Estimation of climate potential We constructed a final multilayer dataset of response and predictor variables for the CONUS including the resulting maps of fractional cover rate of change (four response variables), the mean and slope maps for the climate variables for all the time-lags (70 predictor variables), and the initial percent cover for each lifeform in the year 1986 (four predictor variables). We evaluated for each pixel in the CONUS which of the predictor variables produced the minimum potential rate of change in fractional cover for each lifeform class. To do that, we first calculated the 100% quantile hull of the distribution of each predictor variable against each response variable. To calculate the 100% quantile of the predictor variables’ distribution we divided the total range of each predictor variable into equal-sized bins. The size and number of bins were set specifically per variable due to differences in their data distribution. For each of the bins, we calculated the maximum value of the vegetation rate of change, which resulted in a lookup table with the lower and upper boundaries of each bin, and the associated maximum rate of change. We constructed a total of 296 lookup tables, one per lifeform class and predictor variable combination. The resulting lookup tables were used to construct spatially explicit maps of maximum vegetation rate of change from each of the predictor variable input rasters, and the final climate potential maps were constructed by stacking all the resulting maps per lifeform class and selecting for each pixel the minimum predicted rate of change and the predictor variable that produced that rate. Identifying climate-limited areas We defined climate-limited areas as the parts of the CONUS with little or no differences between the estimated climate potential and the observed rates of change in fractional cover. To identify these areas, we subtracted the raster of observed rates of change from the raster of climate potential for each lifeform class. In the study “CLIMATE-LIMITED VEGETATION CHANGE IN THE CONTERMINOUS UNITED STATES OF AMERICA”, published in the Global Change Biology journal, we evaluated the effects of climate conditions on vegetation composition and distribution in the conterminous United States (CONUS). To disentangle the direct effects of climate change from different non-climate factors, we applied "Liebig's law of the minimum" in a geospatial context, and determined the climate-limited potential for tree, shrub, herbaceous, and non-vegetation fractional cover change. We then compared these potential rates against observed change rates for the period 1986 to 2018 to identify areas of the CONUS where vegetation change is likely being limited by climatic conditions. This dataset contains the input and the resulting rasters for the study which include a) the observed rates of vegetation change, b) the climate derived potential vegetation rates of change, c) the difference between potential and observed values and d) the identified climatic limiting factor.
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2023Embargo end date: 18 Aug 2023Publisher:Zenodo Authors: Hoecker, Tyler;This archive includes a minimal dataset needed to reproduce the analysis as well as a table (CSV) and spatial polygons (ESRI shapefile) of the resulting output from the publication: Hoecker, T.J., S. A. Parks, M. Krosby & S. Z. Dobrowski. 2023. Widespread exposure to altered fire regimes under 2°C warming is projected to transform conifer forests of the Western United States. Communications Earth and Environment. Publication abstract: Changes in wildfire frequency and severity are altering conifer forests and pose threats to biodiversity and natural climate solutions. Where and when feedbacks between vegetation and fire could mediate forest transformation are unresolved. Here, for the western U.S., we used climate analogs to measure exposure to fire-regime change; quantified the direction and spatial distribution of changes in burn severity; and intersected exposure with fire-resistance trait data. We measured exposure as multivariate dissimilarities between contemporary distributions of fire frequency, burn severity, and vegetation productivity and distributions supported by a 2 °C-warmer climate. We project exposure to fire-regime change across 65% of western US conifer forests and mean burn severity to ultimately decline across 63% because of feedbacks with forest productivity and fire frequency. We find that forests occupying disparate portions of climate space are vulnerable to projected fire-regime changes. Forests may adapt to future disturbance regimes, but trajectories remain uncertain.
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visibility 24visibility views 24 download downloads 27 Powered bymore_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2011Embargo end date: 29 Aug 2011Publisher:Harvard Dataverse Authors: E. Kopp, Robert; Golub, Alexander; O. Keohane, Nathaniel; Onda, Chikara;Drawing upon climate change damage functions previously proposed in the literature that we have calibrated to a common level of damages at 2.5 C, we examine the effect upon the social cost of carbon (SCC) of varying the specification of damages in a DICE-like integrated assessment model. In the absence of risk aversion, all of the SCC estimates but one agree within a factor of two. The effect of varying calibration damages is mildly sublinear. With a moderate level of risk aversion included, however, the differences among estimates grow greatly. By combining elements of different damage specifications and roughly taking into account uncertainty in calibration, we have constructed a composite damage function that attempts to approximate the range of uncertainty in climate change damages. In the absence of risk aversion, SCC values calculated with this function are in agreement with the standard quadratic DICE damage function; with a coefficient of relative risk aversion of 1.4, this damage function yields SCC values more than triple those of the standard function.
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2019Embargo end date: 09 May 2019 United StatesPublisher:Data Repository for the University of Minnesota (DRUM) Knoll, Lesley, B.; Sharma, Sapna; Denfeld, Blaize A; Flaim, Giovanna; Hori, Yukari; Magnuson, John J; Straile, Dietmar; Weyhenmeyer, Gesa A;doi: 10.13020/3j5g-kc72
handle: 11299/202813
Lakes and rivers covered by seasonal ice are extensively used by humans. Although ice cover duration has been declining over the past 150 years for Northern Hemisphere lakes and rivers, we still know relatively little about how inland ice loss directly affects humans. Here we provide empirical examples that give quantitative evidence for a winter warming effect on a wide range of cultural ecosystem services. We show that in recent decades, warmer temperatures delayed the opening date of the James Bay winter ice road in northern Ontario, Canada and led to cancellations of religious celebrations (Lake Suwa, Japan and Lake Constance, Germany/Switzerland/Austria), an ice skating race on Lake M��laren, Sweden, and winter ice fishing tournaments in Central and Northern Minnesota. The years with no ice cover on Lake Suwa, Japan from 1443 - 2017. The years with ice cover on Lake Constance, Germany/Switzerland/Austria from 875 - 2018. The years with a normal Vikingar��nnet ice skating race, a modified route, or no race on Lake M��laren, Sweden from 1999 - 2017 as well as associated average winter air temperature. The years with canceled ice fishing tournaments in central and northern Minnesota, USA as well as associated average winter air temperature from 2005 - 2017. Road date openings of the James Bay winter ice road in northern Ontario, Canada and associated freezing degree days from 2005 - 2018.
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Clinical Trial 2019 United StatesPublisher:ClinicalTrials.org A total of 170 participants were initially enrolled in the comprehensive behavioral weight loss intervention.In this study, investigators will conduct a follow-up visit 3 years after the completion of the intervention. Only participants who completed the behavioral weight loss intervention will be enrolled in this study. Participants will undergo testing of body weight, body composition, physical activity patterns, energy intake patterns, sleep patterns, resting metabolic rate, and total daily energy expenditure. This study is designed as an observational trial. The objective of this study is to follow-up with participants 3 years after completion of an 18-month comprehensive behavioral weight loss intervention. Outcomes of interest include change in body weight, body composition, physical activity, energy intake, and sleep. In addition, investigators will explore the associations between current physical activity, sleep, and energy intake patterns and body weight regulation.
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2023Embargo end date: 24 Sep 2023Publisher:Dryad Cresswell, Anna; Renton, Michael; Langlois, Timothy; Thomson, Damian; Lynn, Jasmine; Claudet, Joachim;# Coral reef state influences resilience to acute climate-mediated disturbances\_Table S1 [https://doi.org/10.5061/dryad.rfj6q57gz](https://doi.org/10.5061/dryad.rfj6q57gz) The dataset provides a summary of all publications included in the analysis for this study and the key statistics obtained from the studies and used in the analyses. The dataset includes details about the publication, spatial identifiers (e.g. realm, province, ecoregion) unique site code, information on the disturbance type and timing, the pre-and post-disturbance coral cover, the 5-year annual recovery rate, the recovery shape and recovery completeness classifications. Please see details Methods in the journal article "Coral reef state influences resilience to acute climate-mediated disturbances" as published in Global Ecology and Biogeography. ## Description of the data and file structure Each column provides the following information: | Column | Detail | | ------ | ------ | | Realm | All studies were assigned to an ‘ecoregion’, ‘province’ and ‘realm’ based on their spatial location in Spalding et al. (2007)’s spatial classification system for coastal and shelf waters. | | Province | All studies were assigned to an ‘ecoregion’, ‘province’ and ‘realm’ based on their spatial location in Spalding et al. (2007)’s spatial classification system for coastal and shelf waters. | | Ecoregion | All studies were assigned to an ‘ecoregion’, ‘province’ and ‘realm’ based on their spatial location in Spalding et al. (2007)’s spatial classification system for coastal and shelf waters. | | Unique study identifier | Unique identifiers for the lowest sampling unit in the dataset. In cases where there were data for different regions, reefs, islands/atolls, sites, reef zones, depths, and/or multiple disturbances within a publication or time-series, data from these publications were divided into separate ‘studies’. | | Publication/Dataset | Unique identifiers for the publication or dataset (generally the surname of the first author followed by the year of publication). | | Publication title | Title of the publication or dataset from which the data were sourced. | | Publication year | Year the publication from the which the data were sourced was published. | | Country/Territory | Name of the country or location from which the data came. | | Site latitude | Latitude of the study site from where the data came. | | Site longitude | Longitude of the study site from where the data came. | | Disturbance type | Classification of disturbance: Temperature stress, Cyclone/ severe storm, Runoff or Multiple. | | Disturbance.year | Year of the disturbance. | | Mean coral cover pre-disturbance | Pre-disturbance coral cover as extracted from the publication or dataset as the closest data point prior to disturbance. If there is an NA value in this column then there was no pre-disturbance data available and a measure of impact was not calculated. | | Mean coral cover post-disturbance | Post-disturbance coral cover as extracted from the publication or dataset as the closest data point prior to disturbance. If there is an NA value in this column then there was no pre-disturbance data available and a measure of impact was not calculated. | | Impact (lnRR) | Impact measure: the log response ratio of pre- to post-disturbance percentage coral cover. If there is an NA value in this column then there was no pre-disturbance data available and a measure of impact was not calculated. | | Time-averaged recovery rate | Recovery rate as percentage coral cover per year in the approximate 5-year time window following disturbance. See main Methods text in manuscript for more detail. If there is an NA value in this column then the available time-series following disturbance did not satisfy the criteria for inclusion in the calculation of recovery rate. | | Recovery shape | Recovery shape category: linear, accelerating, decelerating, logistic, flatline or null. If there is an NA value in this column then the available time-series following disturbance did not satisfy the criteria for inclusion in classification of recovery shape. | | Recovery completeness | Recovery completeness category: complete recovery – coral is observed to reach its pre-disturbance coral cover, signs of recovery – a positive trajectory but not reaching pre-disturbance cover in the time period examined, undetermined – no clear pattern in recovery, the null model was the top model, no recovery – the null model was the top model but the linear model had slope and standard error in slope near zero and further decline – the top model had a negative trend. If there is an NA value in this column then the available time-series following disturbance did not satisfy the criteria for inclusion in classification of recovery shape. | | Reference | Source for the data. | ## Sharing/Access information Data was derived from the following sources: **Appendix 1. Full list of references providing the data used in impact and recovery analyses supporting Table S1** Arceo, H. O., Quibilan, M. C., Aliño, P. M., Lim, G., & Licuanan, W. Y. (2001). Coral bleaching in Philippine reefs: Coincident evidences with mesoscale thermal anomalies. Bulletin of Marine Science, 69(2), 579-593. Aronson, R. B., Precht, W. F., Toscano, M. A., & Koltes, K. H. (2002). The 1998 bleaching event and its aftermath on a coral reef in Belize. Marine Biology, 141(3), 435-447. Aronson, R. B., Sebens, K. P., & Ebersole, J. P. (1994). Hurricane Hugo's impact on Salt River submarine canyon, St. Croix, US Virgin Islands. Proceedings of the colloquium on global aspects of coral reefs, Miami, 1993, 189-195. Bahr, K. D., Rodgers, K. S., & Jokiel, P. L. (2017). Impact of three bleaching events on the reef resiliency of Kāne'ohe Bay, Hawai'i. Frontiers in Marine Science, 4(DEC). Baird, A. H., Álvarez-Noriega, M., Cumbo, V. R., Connolly, S. R., Dornelas, M., & Madin, J. S. (2018). Effects of tropical storms on the demography of reef corals. Marine Ecology Progress Series, 606, 29-38. Barranco, L. M., Carriquiry, J. D., Rodríguez-Zaragoza, F. A., Cupul-Magaña, A. L., Villaescusa, J. A., & Calderón-Aguilera, L. E. (2016). Spatiotemporal variations of live coral cover in the Northern Mesoamerican reef system, Yucatan Peninsula, Mexico. Scientia Marina, 80(2), 143-150. Bastidas, C., Bone, D., Croquer, A., Debrot, D., Garcia, E., Humanes, A., . . . Rodríguez, S. (2012). Massive hard coral loss after a severe bleaching event in 2010 at Los Roques, Venezuela. Revista de Biologia Tropical, 60(SUPPL. 1), 29-37. Booth, D. J., & Beretta, G. A. (2002). Changes in a fish assemblage after a coral bleaching event. Marine Ecology Progress Series, 245, 205-212. Brandl, S. J., Emslie, M. J., & Ceccarelli, D. M. (2016). Habitat degradation increases functional originality in highly diverse coral reef fish assemblages. Ecosphere, 7(11). Brown, D., & Edmunds, P. J. (2013). Long-term changes in the population dynamics of the Caribbean hydrocoral Millepora spp. Journal of Experimental Marine Biology and Ecology, 441, 62-70. Brown, V. B., Davies, S. A., & Synnot, R. N. (1990). Long-term Monitoring of the Effects of Treated Sewage Effluent on the Intertidal Macroalgal Community Near Cape Schanck, Victoria, Australia. Botanica Marina, 33(1), 85-98. Bruckner, A. W., Coward, G., Bimson, K., & Rattanawongwan, T. (2017). Predation by feeding aggregations of Drupella spp. inhibits the recovery of reefs damaged by a mass bleaching event. Coral Reefs, 36(4), 1181-1187. Burt, J. 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Status of Caribbean coral reefs after bleaching and hurricanes in 2005. Wismer, S., Tebbett, S. B., Streit, R. P., & Bellwood, D. R. (2019). Spatial mismatch in fish and coral loss following 2016 mass coral bleaching. Science of the Total Environment, 650, 1487-1498. Woolsey, E., Bainbridge, S. J., Kingsford, M. J., & Byrne, M. (2012). Impacts of cyclone Hamish at One Tree Reef: Integrating environmental and benthic habitat data. Marine Biology, 159(4), 793-803. Aim: Understand the interplay between resistance and recovery on coral reefs, and investigate dependence on pre- and post-disturbance states, to inform generalisable reef resilience theory across large spatial and temporal scales. Location: Tropical coral reefs globally. Time period: 1966 to 2017. Major taxa studied: Scleratinian hard corals. Methods: We conducted a literature search to compile a global dataset of total coral cover before and after acute storms, temperature stress, and coastal runoff from flooding events. We used meta-regression to identify variables that explained significant variation in disturbance impact, including disturbance type, year, depth, and pre-disturbance coral cover. We further investigated the influence of these same variables, as well as post-disturbance coral cover and disturbance impact, on recovery rate. We examined the shape of recovery, assigning qualitatively distinct, ecologically relevant, population growth trajectories: linear, logistic, logarithmic (decelerating), and a second-order quadratic (accelerating). Results: We analysed 427 disturbance impacts and 117 recovery trajectories. Accelerating and logistic were the most common recovery shapes, underscoring non-linearities and recovery lags. A complex but meaningful relationship between the state of a reef pre- and post-disturbance, disturbance impact magnitude, and recovery rate was identified. Fastest recovery rates were predicted for intermediate to large disturbance impacts, but a decline in this rate was predicted when more than ~75% of pre-disturbance cover was lost. We identified a shifting baseline, with declines in both pre-and post-disturbance coral cover over the 50 year study period. Main conclusions: We breakdown the complexities of coral resilience, showing interplay between resistance and recovery, as well as dependence on both pre- and post-disturbance states, alongside documenting a chronic decline in these states. This has implications for predicting coral reef futures and implementing actions to enhance resilience. The dataset provides a summary of all studies included in the analysis and the key statistics obtained from the studies and used in the analyses for the manuscript entitled "Coral reef state influences resilience to acute climate-mediated disturbances" as published in Global Ecology and Biogeography. The dataset includes details about the publication, spatial identifiers (e.g. realm, province, ecoregion) unique site code, information on the disturbance type and timing, the pre-and post-disturbance coral cover, the 5-year annual recovery rate, the recovery shape and recovery completeness classifications. Please see details Methods in the journal article "Coral reef state influences resilience to acute climate-mediated disturbances" as published in Global Ecology and Biogeography.
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2018Embargo end date: 10 Jan 2019Publisher:Dryad Pang, Rich; Van Breugel, Floris; Dickinson, Michael; Riffell, Jeffrey A.; Fairhall, Adrienne;doi: 10.5061/dryad.n0b8m
Flight trajectories of fruit flies and mosquitoes in a wind tunnel.This data file is a MySQL database file which must be uploaded to a MySQL database management system (DBMS) (e.g., via the MAMP installation: http://localhost:8888/MAMP/?language=English, as was used in the associated manuscript). Once you have installed a MySQL DBMS on your machine, make a new database called “wind_tunnel_db”. To populate this database using the data file, first download all of the data files and join them together using: cat wind_tunnel_db_* > wind_tunnel_db.sql Then run the following command to populate the wind_tunnel_db MySQL database with the result. /path/to/mysql -uroot -proot wind_tunnel_db < /path/to/wind_tunnel_db.sql replacing the paths and username/passwords as appropriate. It will take several minutes since it is a large file. The database contains several tables, which are mostly self explanatory. The key tables of interest are the “experiment” table, which lists the 4 experiments contained in this data set, the “timepoint” table, which contains the position, velocity, etc., of every fly/mosquito at every measured time point, and the “trajectory” table, which indicates which set of time points correspond to which individual trajectories. Other useful tables that have been pre-populated are the “crossing” table, which specifies trajectory segments corresponding to each plume crossing, and the “crossing_group” table, which groups sets of crossings together according to experiment and crossing identification criteria. The code that interacts with this database and recreates the figures in the associated manuscript is contained at https://github.com/rkp8000/wind_tunnel.wind_tunnel_db_aaPart 2wind_tunnel_db_abPart 3wind_tunnel_db_acPart 4wind_tunnel_db_adPart 5wind_tunnel_db_aePart 6wind_tunnel_db_afPart 7wind_tunnel_db_agPart 8wind_tunnel_db_ahPart 9wind_tunnel_db_aiInfotaxis databaseBase database for running infotaxis simulations. To see how to prepare and populate this database with simulated trajectory data, see the file _paper_auxiliary_code in the GitHub repository http://github.com/rkp8000/wind_tunnel.infotaxis_db.sql Natural decision-making often involves extended decision sequences in response to variable stimuli with complex structure. As an example, many animals follow odor plumes to locate food sources or mates, but turbulence breaks up the advected odor signal into intermittent filaments and puffs. This scenario provides an opportunity to ask how animals use sparse, instantaneous, and stochastic signal encounters to generate goal-oriented behavioral sequences. Here we examined the trajectories of flying fruit flies (Drosophila melanogaster) and mosquitoes (Aedes aegypti) navigating in controlled plumes of attractive odorants. While it is known that mean odor-triggered flight responses are dominated by upwind turns, individual responses are highly variable. We asked whether deviations from mean responses depended on specific features of odor encounters, and found that odor-triggered turns were slightly but significantly modulated by two features of odor encounters. First, encounters with higher concentrations triggered stronger upwind turns. Second, encounters occurring later in a sequence triggered weaker upwind turns. To contextualize the latter history dependence theoretically, we examined trajectories simulated from three normative tracking strategies. We found that neither a purely reactive strategy nor a strategy in which the tracker learned the plume centerline over time captured the observed history dependence. In contrast, “infotaxis”, in which flight decisions maximized expected information gain about source location, exhibited a history dependence aligned in sign with the data, though much larger in magnitude. These findings suggest that while true plume tracking is dominated by a reactive odor response it might also involve a history-dependent modulation of responses consistent with the accumulation of information about a source over multi-encounter timescales. This suggests that short-term memory processes modulating decision sequences may play a role in natural plume tracking.
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2023Publisher:Zenodo Authors: Markus Stoffel; Daniel G. Trappmann; Mattias I. Coullie; Juan A. Ballesteros-Cánovas; +1 AuthorsMarkus Stoffel; Daniel G. Trappmann; Mattias I. Coullie; Juan A. Ballesteros-Cánovas; Christophe Corona;This readme file provides all data and R codes used to perform the analyses presented in Figs. 2-4 of the main text and Supplementary Information Figures S1-S2-S3. FIGURE 2 - Seasonally_dated_GDs.txt: Contains information on the timing (Season) of rockfall (GD) in a given tree (Id) and a given year (yr) over the past 100 years. Inv refers to the operators which analyzed growth disturbances in the tree-ring series. Lat / Long refers to the position of the tree in CH1903/ Swiss Grid projection. Intensity (1-4) refers to (1), intermediate (2) and strong (3) GD. Intensity 4 was attributed to injuries (I). Only the 408 GD rated 3 (strong TRD) and 4 (injuries) were used in Fig. 2. Acronyms used for Response_type read as follows: TRD: Tangential rows of traumatic resin ducts; I: Injuries. Acronyms used for Season refer to Dormancy (1_D), early (2_EE), middle (3_ME) and late (4_LE) earlywood, whereas a GD found in the latewood was attributed to either the early (5_EL) or late (6_LL) latewood. - Trends_in_seasonality_R1.R: The data contained in "Seasonally_dated_GDs" were processed with the R script "Trends_in_Seasonality.R". This seasonal trend analysis code is inspired by work published by Schlögl et al. (2021; https://doi.org/10.1016/j.crm.2021.100294) and Heiser et al. (2022; https://doi.org/10.1029/2011JF002262). FIGURE 3-4-S1 - Tasch_GD.txt: Contains the raw data on rockfall impacts (GD) in a given year (yr) as found in all trees available in that same year (Sample_depth) as well as the cumulated diameter at breast height (cumulated_DBH) of all trees present in that same year. - Rockfall_frequency_climate.R: The data contained in "Tasch_GD.txt" were processed with the R script "Rockfall_frequency_climate.R". - The temperature (Imfeld23_tmp.txt) and precipitation (Imfeld23_prc.txt) data used in Fig. 3 are from the Imfeld et al. 2023 (10.5194/cp-19-703-2023) gridded dataset (1x1 km lat/long) and were extracted at the grid point centered on the Täschgufer site. - The script set with temperature series enables to compute Fig. 4 (l.149:216) and Fig. 3 (l. 216:330); the script set with precipitation series enables to compute Fig. S1 FIGURE S2 - Tasch_GD.txt: Contains the raw data on rockfall impacts (GD) at the Täschgufer site in a given year (yr) as found in all trees available in that same year (Sample_depth) as well as the cumulated diameter at breast height (cumulated_DBH) of all trees present in that same year. - Rockfall_frequency_borehole.R: is adapted from "Rockfall_frequency_climate.R" to work with the borehole dates. - Corvatsch0_6R1: Contains the Corvatsch borehole temperature series (2000-2020, 0.6m depth) (Hoelzle, M. et al. https://doi.org/10.5194/essd-14-1531-2022, 2022). FIGURE S3 - Plattje_GD.txt: Contains the raw data on rockfall impacts (GD) at the Plattje site in a given year (yr) as found all trees available in that same year (Sample_depth) as well as the cumulated diameter at breast height (cumulated_DBH) of all trees present in that same year. - - Rockfall_frequency_climate_Plattje.R: The data contained in "Plattje_GD.txt" were processed with the R script "Rockfall_frequency_climate_Plattje.R". - The temperature (Imfeld23_tmp_Plattje.txt) and precipitation (Imfeld23_prc_Plattje.txt) data used in Fig. 3 are from Imfeld et al. 2023 (10.5194/cp-19-703-2023) gridded dataset (1x1 km lat/long) and were extracted at the grid point centered on the Plattje site.
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Research data keyboard_double_arrow_right Dataset 2023Publisher:Zenodo Authors: Matteo, Nigro; Michele, Barsanti; Roberto, Giannecchini;The version 1.0 contains the supporting data for the work (still under submission) "Last century changes in annual precipitation in a Mediterranean area and their spatial variability. Insights from northern Tuscany (Italy)". The following files are here available (all file are georeferenced in EPSG: 3003): - AVG_Rainfall_1990-2019.tif -> Raster map of the mean annual precipitation for the northern Tuscany, Italy. It encompasses the portion of the Tuscany region northern of the cities of Livorno - Florence. The interpolation was validated via a leave one out cross-validation procedure. - D3-1_Area2_ApuanAlps.tif -> Raster map of the differences in mean annual precipitation between the two 3-decades periods 1921 to 1950 and 1990 to 2019 for the Apuan Alps mountain ridge (Tuscany, Italy). - D3-2_Area2_ApuanAlps.tif -> Raster map of the differences in mean annual precipitation between the two 3-decades periods 1951 to 1980 and 1990 to 2019 for the Apuan Alps mountain ridge (Tuscany, Italy). - DeltaSHP_Points_AVG_Annual_Rainfall.zip -> Shape file of the raingauges locations with the mean annual precipitation values of the period 1990 to 2019. - RaingaugesSHP_Points_AVG_Annual_Rainfall_1990-2019.zip -> Shape file of the raingauges locations with the following information: differences in the mean annual precipitation values between the two 3-decades periods 1951 to 1980 and 1990 to 2019 (named D3-2); p values of the t-test for significance of the differences between the mean annual precipitation ofthe two 3-decades periods 1951 to 1980 and 1990 to 2019; difference in the mean annual precipitation values between the two 3-decades periods 1921 to 1950 and 1990 to 2019 (named D3-1); p values of the t-test for significance of the differences between the mean annual precipitation ofthe two 3-decades periods 1921 to 1950 and 1990 to 2019.
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2016Publisher:Zenodo Authors: Ruest, Nick;Consists of a web crawl of unique URLs tweeted with the #YMMFire hashtag. #YMMFire collection took place from May 1-June 25, 2016. Unique URLs were extracted from the dataset, and harvested with Heritrix on August 31-September 2, 2017. This research was supported by a research grant -- 435-2015-0011 -- issued by Social Sciences and Humanities Research Council.
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You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2024Embargo end date: 05 Mar 2024Publisher:Dryad Authors: Parra, Adriana; Greenberg, Jonathan;This README file was generated on 2024-03-04 by Adriana Parra. ## GENERAL INFORMATION 1\. Title of Dataset: **Climate-limited vegetation change in the conterminous United States of America** 2\. Author Information A. First Author Contact Information Name: Adriana Parra Institution: University of Nevada, Reno Address: Reno, NV USA Email: adrianaparra@unr.edu B. Co-author Contact Information Name: Jonathan Greenberg Institution: University of Nevada, Reno Address: Reno, NV USA Email: jgreenberg@unr.edu 3\. Coverage period of the dataset: 1986-2018 4\. Geographic location of dataset: Conterminous United States 5\. Description: This dataset contains the input and the resulting rasters for the study “CLIMATE-LIMITED VEGETATION CHANGE IN THE CONTERMINOUS UNITED STATES OF AMERICA”, published in the Global Change Biology journal. The dataset includes a) the observed rates of vegetation change, b) the climate derived potential vegetation rates of change, c) the difference between potential and observed values and d) the identified climatic limiting factor. Additionally, the dataset includes a legend file for the identified climatic limiting factor rasters. ## SHARING/ACCESS INFORMATION 1\. Links to publications that cite or use the data: **Parra, A., & Greenberg, J. (2024). Climate-limited vegetation change in the conterminous United States of America. Global Change Biology, 30, e17204. [https://doi.org/10.1111/gcb.17204](https://doi.org/10.1111/gcb.17204)** 2\. Links to other publicly accessible locations of the data: None 3\. Links/relationships to ancillary data sets: None 4\. Was data derived from another source? Yes A. If yes, list source(s): "Vegetative Lifeform Cover from Landsat SR for CONUS" product publicly available in the ORNL DAAC (https://daac.ornl.gov/cgi-bin/dsviewer.pl?ds_id=1809) TerraClimate data catalog publicly available at the website https://www.climatologylab.org/terraclimate.html 5\. Recommended citation for this dataset: Parra, A., & Greenberg, J. (2024). Climate-limited vegetation change in the conterminous United States of America. Global Change Biology, 30, e17204. [https://doi.org/10.1111/gcb.17204](https://doi.org/10.1111/gcb.17204) ## DATA & FILE OVERVIEW This dataset contains 16 geotiff files, and one csv file. There are 4 geotiff files per each of the lifeform classes evaluated in this study: herbaceous, tree, shrub, and non-vegetation. The files corresponding to each lifeform class are indicated by the first two letters in the file name, HC indicates herbaceous cover, TC indicates tree cover, SC indicates shrub cover, and NC indicates non-vegetation cover. 1\. File List: a) Observed change: Trends of vegetation change between 1986 and 2018. b) Potential predict: Predicted rates of vegetation change form the climate limiting factor analysis. c) Potential observed difference: Difference between the potential and the observed vegetation rates of change. d) Limiting variable: Climate variable identified as the limiting factor for each pixel the conterminous United States. e) Legend of the Limiting variable raster All the geotiff files are stored as Float 32 type, and in CONUS Albers Equal Area coordinate system (EPSG:5070) The csv file included in the dataset is the legend for the limiting variable geotiff files. This file includes the name of the climate variable corresponding to each number in the limiting variable files, as well as information on the variable type and the corresponding time lag. 2\. Relationship between files, if important: None 3\. Additional related data collected that was not included in the current data package: None 4\. Are there multiple versions of the dataset? No A. If yes, name of file(s) that was updated: NA i. Why was the file updated? NA ii. When was the file updated? NA Input data We use the available data from the “Vegetative Lifeform Cover from Landsat SR for CONUS” product (https://daac.ornl.gov/cgi-bin/dsviewer.pl?ds_id=1809) to evaluate the changes in vegetation fractional cover. The information for the climate factors was derived from the TerraClimate data catalog (https://www.climatologylab.org/terraclimate.html). We downloaded data from this catalog for the period 1971 to 2018 for the following variables: minimum temperature (TMIN), precipitation (PPT), actual evapotranspiration (AET), potential evapotranspiration (PET), and climatic water deficit (DEF). Preprocessing of vegetation fractional cover data We resampled and aligned the maps of fractional cover using pixel averaging to the extent and resolution of the TerraClimate dataset (~ 4 km). Then, we calculated rates of lifeform cover change per pixel using the Theil-Sen slope analysis (Sen, 1968; Theil, 1992). Preprocessing of climate variables data To process the climate data, we defined a year time step as the months from July of one year to July of the next. Following this definition, we constructed annual maps of each climate variable for the years 1971 to 2018. The annual maps of each climate variable were further summarized per pixel, into mean and slope (calculated as the Theil-Sen slope) across one, two, three, four, five, ten-, and 15-year lags. Estimation of climate potential We constructed a final multilayer dataset of response and predictor variables for the CONUS including the resulting maps of fractional cover rate of change (four response variables), the mean and slope maps for the climate variables for all the time-lags (70 predictor variables), and the initial percent cover for each lifeform in the year 1986 (four predictor variables). We evaluated for each pixel in the CONUS which of the predictor variables produced the minimum potential rate of change in fractional cover for each lifeform class. To do that, we first calculated the 100% quantile hull of the distribution of each predictor variable against each response variable. To calculate the 100% quantile of the predictor variables’ distribution we divided the total range of each predictor variable into equal-sized bins. The size and number of bins were set specifically per variable due to differences in their data distribution. For each of the bins, we calculated the maximum value of the vegetation rate of change, which resulted in a lookup table with the lower and upper boundaries of each bin, and the associated maximum rate of change. We constructed a total of 296 lookup tables, one per lifeform class and predictor variable combination. The resulting lookup tables were used to construct spatially explicit maps of maximum vegetation rate of change from each of the predictor variable input rasters, and the final climate potential maps were constructed by stacking all the resulting maps per lifeform class and selecting for each pixel the minimum predicted rate of change and the predictor variable that produced that rate. Identifying climate-limited areas We defined climate-limited areas as the parts of the CONUS with little or no differences between the estimated climate potential and the observed rates of change in fractional cover. To identify these areas, we subtracted the raster of observed rates of change from the raster of climate potential for each lifeform class. In the study “CLIMATE-LIMITED VEGETATION CHANGE IN THE CONTERMINOUS UNITED STATES OF AMERICA”, published in the Global Change Biology journal, we evaluated the effects of climate conditions on vegetation composition and distribution in the conterminous United States (CONUS). To disentangle the direct effects of climate change from different non-climate factors, we applied "Liebig's law of the minimum" in a geospatial context, and determined the climate-limited potential for tree, shrub, herbaceous, and non-vegetation fractional cover change. We then compared these potential rates against observed change rates for the period 1986 to 2018 to identify areas of the CONUS where vegetation change is likely being limited by climatic conditions. This dataset contains the input and the resulting rasters for the study which include a) the observed rates of vegetation change, b) the climate derived potential vegetation rates of change, c) the difference between potential and observed values and d) the identified climatic limiting factor.
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2023Embargo end date: 18 Aug 2023Publisher:Zenodo Authors: Hoecker, Tyler;This archive includes a minimal dataset needed to reproduce the analysis as well as a table (CSV) and spatial polygons (ESRI shapefile) of the resulting output from the publication: Hoecker, T.J., S. A. Parks, M. Krosby & S. Z. Dobrowski. 2023. Widespread exposure to altered fire regimes under 2°C warming is projected to transform conifer forests of the Western United States. Communications Earth and Environment. Publication abstract: Changes in wildfire frequency and severity are altering conifer forests and pose threats to biodiversity and natural climate solutions. Where and when feedbacks between vegetation and fire could mediate forest transformation are unresolved. Here, for the western U.S., we used climate analogs to measure exposure to fire-regime change; quantified the direction and spatial distribution of changes in burn severity; and intersected exposure with fire-resistance trait data. We measured exposure as multivariate dissimilarities between contemporary distributions of fire frequency, burn severity, and vegetation productivity and distributions supported by a 2 °C-warmer climate. We project exposure to fire-regime change across 65% of western US conifer forests and mean burn severity to ultimately decline across 63% because of feedbacks with forest productivity and fire frequency. We find that forests occupying disparate portions of climate space are vulnerable to projected fire-regime changes. Forests may adapt to future disturbance regimes, but trajectories remain uncertain.
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2011Embargo end date: 29 Aug 2011Publisher:Harvard Dataverse Authors: E. Kopp, Robert; Golub, Alexander; O. Keohane, Nathaniel; Onda, Chikara;Drawing upon climate change damage functions previously proposed in the literature that we have calibrated to a common level of damages at 2.5 C, we examine the effect upon the social cost of carbon (SCC) of varying the specification of damages in a DICE-like integrated assessment model. In the absence of risk aversion, all of the SCC estimates but one agree within a factor of two. The effect of varying calibration damages is mildly sublinear. With a moderate level of risk aversion included, however, the differences among estimates grow greatly. By combining elements of different damage specifications and roughly taking into account uncertainty in calibration, we have constructed a composite damage function that attempts to approximate the range of uncertainty in climate change damages. In the absence of risk aversion, SCC values calculated with this function are in agreement with the standard quadratic DICE damage function; with a coefficient of relative risk aversion of 1.4, this damage function yields SCC values more than triple those of the standard function.
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2019Embargo end date: 09 May 2019 United StatesPublisher:Data Repository for the University of Minnesota (DRUM) Knoll, Lesley, B.; Sharma, Sapna; Denfeld, Blaize A; Flaim, Giovanna; Hori, Yukari; Magnuson, John J; Straile, Dietmar; Weyhenmeyer, Gesa A;doi: 10.13020/3j5g-kc72
handle: 11299/202813
Lakes and rivers covered by seasonal ice are extensively used by humans. Although ice cover duration has been declining over the past 150 years for Northern Hemisphere lakes and rivers, we still know relatively little about how inland ice loss directly affects humans. Here we provide empirical examples that give quantitative evidence for a winter warming effect on a wide range of cultural ecosystem services. We show that in recent decades, warmer temperatures delayed the opening date of the James Bay winter ice road in northern Ontario, Canada and led to cancellations of religious celebrations (Lake Suwa, Japan and Lake Constance, Germany/Switzerland/Austria), an ice skating race on Lake M��laren, Sweden, and winter ice fishing tournaments in Central and Northern Minnesota. The years with no ice cover on Lake Suwa, Japan from 1443 - 2017. The years with ice cover on Lake Constance, Germany/Switzerland/Austria from 875 - 2018. The years with a normal Vikingar��nnet ice skating race, a modified route, or no race on Lake M��laren, Sweden from 1999 - 2017 as well as associated average winter air temperature. The years with canceled ice fishing tournaments in central and northern Minnesota, USA as well as associated average winter air temperature from 2005 - 2017. Road date openings of the James Bay winter ice road in northern Ontario, Canada and associated freezing degree days from 2005 - 2018.
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Clinical Trial 2019 United StatesPublisher:ClinicalTrials.org A total of 170 participants were initially enrolled in the comprehensive behavioral weight loss intervention.In this study, investigators will conduct a follow-up visit 3 years after the completion of the intervention. Only participants who completed the behavioral weight loss intervention will be enrolled in this study. Participants will undergo testing of body weight, body composition, physical activity patterns, energy intake patterns, sleep patterns, resting metabolic rate, and total daily energy expenditure. This study is designed as an observational trial. The objective of this study is to follow-up with participants 3 years after completion of an 18-month comprehensive behavioral weight loss intervention. Outcomes of interest include change in body weight, body composition, physical activity, energy intake, and sleep. In addition, investigators will explore the associations between current physical activity, sleep, and energy intake patterns and body weight regulation.
add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.eu0 citations 0 popularity Average influence Average impulse Average Powered by BIP!
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2023Embargo end date: 24 Sep 2023Publisher:Dryad Cresswell, Anna; Renton, Michael; Langlois, Timothy; Thomson, Damian; Lynn, Jasmine; Claudet, Joachim;# Coral reef state influences resilience to acute climate-mediated disturbances\_Table S1 [https://doi.org/10.5061/dryad.rfj6q57gz](https://doi.org/10.5061/dryad.rfj6q57gz) The dataset provides a summary of all publications included in the analysis for this study and the key statistics obtained from the studies and used in the analyses. The dataset includes details about the publication, spatial identifiers (e.g. realm, province, ecoregion) unique site code, information on the disturbance type and timing, the pre-and post-disturbance coral cover, the 5-year annual recovery rate, the recovery shape and recovery completeness classifications. Please see details Methods in the journal article "Coral reef state influences resilience to acute climate-mediated disturbances" as published in Global Ecology and Biogeography. ## Description of the data and file structure Each column provides the following information: | Column | Detail | | ------ | ------ | | Realm | All studies were assigned to an ‘ecoregion’, ‘province’ and ‘realm’ based on their spatial location in Spalding et al. (2007)’s spatial classification system for coastal and shelf waters. | | Province | All studies were assigned to an ‘ecoregion’, ‘province’ and ‘realm’ based on their spatial location in Spalding et al. (2007)’s spatial classification system for coastal and shelf waters. | | Ecoregion | All studies were assigned to an ‘ecoregion’, ‘province’ and ‘realm’ based on their spatial location in Spalding et al. (2007)’s spatial classification system for coastal and shelf waters. | | Unique study identifier | Unique identifiers for the lowest sampling unit in the dataset. In cases where there were data for different regions, reefs, islands/atolls, sites, reef zones, depths, and/or multiple disturbances within a publication or time-series, data from these publications were divided into separate ‘studies’. | | Publication/Dataset | Unique identifiers for the publication or dataset (generally the surname of the first author followed by the year of publication). | | Publication title | Title of the publication or dataset from which the data were sourced. | | Publication year | Year the publication from the which the data were sourced was published. | | Country/Territory | Name of the country or location from which the data came. | | Site latitude | Latitude of the study site from where the data came. | | Site longitude | Longitude of the study site from where the data came. | | Disturbance type | Classification of disturbance: Temperature stress, Cyclone/ severe storm, Runoff or Multiple. | | Disturbance.year | Year of the disturbance. | | Mean coral cover pre-disturbance | Pre-disturbance coral cover as extracted from the publication or dataset as the closest data point prior to disturbance. If there is an NA value in this column then there was no pre-disturbance data available and a measure of impact was not calculated. | | Mean coral cover post-disturbance | Post-disturbance coral cover as extracted from the publication or dataset as the closest data point prior to disturbance. If there is an NA value in this column then there was no pre-disturbance data available and a measure of impact was not calculated. | | Impact (lnRR) | Impact measure: the log response ratio of pre- to post-disturbance percentage coral cover. If there is an NA value in this column then there was no pre-disturbance data available and a measure of impact was not calculated. | | Time-averaged recovery rate | Recovery rate as percentage coral cover per year in the approximate 5-year time window following disturbance. See main Methods text in manuscript for more detail. If there is an NA value in this column then the available time-series following disturbance did not satisfy the criteria for inclusion in the calculation of recovery rate. | | Recovery shape | Recovery shape category: linear, accelerating, decelerating, logistic, flatline or null. If there is an NA value in this column then the available time-series following disturbance did not satisfy the criteria for inclusion in classification of recovery shape. | | Recovery completeness | Recovery completeness category: complete recovery – coral is observed to reach its pre-disturbance coral cover, signs of recovery – a positive trajectory but not reaching pre-disturbance cover in the time period examined, undetermined – no clear pattern in recovery, the null model was the top model, no recovery – the null model was the top model but the linear model had slope and standard error in slope near zero and further decline – the top model had a negative trend. If there is an NA value in this column then the available time-series following disturbance did not satisfy the criteria for inclusion in classification of recovery shape. | | Reference | Source for the data. | ## Sharing/Access information Data was derived from the following sources: **Appendix 1. Full list of references providing the data used in impact and recovery analyses supporting Table S1** Arceo, H. O., Quibilan, M. C., Aliño, P. M., Lim, G., & Licuanan, W. Y. (2001). Coral bleaching in Philippine reefs: Coincident evidences with mesoscale thermal anomalies. Bulletin of Marine Science, 69(2), 579-593. Aronson, R. B., Precht, W. F., Toscano, M. A., & Koltes, K. H. (2002). The 1998 bleaching event and its aftermath on a coral reef in Belize. Marine Biology, 141(3), 435-447. Aronson, R. B., Sebens, K. P., & Ebersole, J. P. (1994). Hurricane Hugo's impact on Salt River submarine canyon, St. Croix, US Virgin Islands. Proceedings of the colloquium on global aspects of coral reefs, Miami, 1993, 189-195. Bahr, K. D., Rodgers, K. S., & Jokiel, P. L. (2017). Impact of three bleaching events on the reef resiliency of Kāne'ohe Bay, Hawai'i. Frontiers in Marine Science, 4(DEC). Baird, A. H., Álvarez-Noriega, M., Cumbo, V. R., Connolly, S. R., Dornelas, M., & Madin, J. S. (2018). Effects of tropical storms on the demography of reef corals. Marine Ecology Progress Series, 606, 29-38. Barranco, L. M., Carriquiry, J. D., Rodríguez-Zaragoza, F. A., Cupul-Magaña, A. L., Villaescusa, J. A., & Calderón-Aguilera, L. E. (2016). Spatiotemporal variations of live coral cover in the Northern Mesoamerican reef system, Yucatan Peninsula, Mexico. Scientia Marina, 80(2), 143-150. Bastidas, C., Bone, D., Croquer, A., Debrot, D., Garcia, E., Humanes, A., . . . Rodríguez, S. (2012). Massive hard coral loss after a severe bleaching event in 2010 at Los Roques, Venezuela. Revista de Biologia Tropical, 60(SUPPL. 1), 29-37. Booth, D. J., & Beretta, G. A. (2002). Changes in a fish assemblage after a coral bleaching event. Marine Ecology Progress Series, 245, 205-212. Brandl, S. J., Emslie, M. J., & Ceccarelli, D. M. (2016). Habitat degradation increases functional originality in highly diverse coral reef fish assemblages. Ecosphere, 7(11). Brown, D., & Edmunds, P. J. (2013). Long-term changes in the population dynamics of the Caribbean hydrocoral Millepora spp. Journal of Experimental Marine Biology and Ecology, 441, 62-70. Brown, V. B., Davies, S. A., & Synnot, R. N. (1990). Long-term Monitoring of the Effects of Treated Sewage Effluent on the Intertidal Macroalgal Community Near Cape Schanck, Victoria, Australia. Botanica Marina, 33(1), 85-98. Bruckner, A. W., Coward, G., Bimson, K., & Rattanawongwan, T. (2017). Predation by feeding aggregations of Drupella spp. inhibits the recovery of reefs damaged by a mass bleaching event. Coral Reefs, 36(4), 1181-1187. Burt, J. 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Reef resilience and change 1998–2007, Alphonse Atoll, Seychelles. Paper presented at the Proc 11th Int Coral Reef Symp. Harii, S., Hongo, C., Ishihara, M., Ide, Y., & Kayanne, H. (2014). Impacts of multiple disturbances on coral communities at Ishigaki Island, Okinawa, Japan, during a 15 year survey. Marine Ecology Progress Series, 509, 171-180. Harrison, H. B., Álvarez-Noriega, M., Baird, A. H., Heron, S. F., MacDonald, C., & Hughes, T. P. (2018). Back-to-back coral bleaching events on isolated atolls in the Coral Sea. Coral Reefs. Holbrook, S. J., Adam, T. C., Edmunds, P. J., Schmitt, R. J., Carpenter, R. C., Brooks, A. J., . . . Briggs, C. J. (2018). Recruitment Drives Spatial Variation in Recovery Rates of Resilient Coral Reefs. Scientific Reports, 8(1). Hongo, C., & Yamano, H. (2013). Species-Specific Responses of Corals to Bleaching Events on Anthropogenically Turbid Reefs on Okinawa Island, Japan, over a 15-year Period (1995-2009). PLoS ONE, 8(4). 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Long-term change in bioconstruction potential of Maldivian coral reefs following extreme climate anomalies. Global Change Biology, 24(12), 5629-5641. Morgan, K. M., Perry, C. T., Johnson, J. A., & Smithers, S. G. (2017). Nearshore turbid-zone corals exhibit high bleaching tolerance on the Great Barrier Reef following the 2016 ocean warming event. Frontiers in Marine Science, 4. Obura, D., Gudka, M., Rabi, F. A., Gian, S. B., Bijoux, J., Freed, S., . . . Sola, E. (2017). Coral Reef Status Report for the Western Indian Ocean (2017). Paper presented at the Nairobi Convention. Obura, D., & Mangubhai, S. (2011). Coral mortality associated with thermal fluctuations in the Phoenix Islands, 2002-2005. Coral Reefs, 30(3), 607-619. Ostrander, G. K., Armstrong, K. M., Knobbe, E. T., Gerace, D., & Scully, E. P. (2000). Rapid transition the structure of a coral reef community: The effects of coral bleaching and physical disturbance. Proceedings of the National Academy of Sciences of the United States of America, 97(10), 5297-5302. Pereira, M. A. M., & Gonçalves, P. M. B. (2004). Effects of the 2000 southern Mozambique floods on a marginal coral community: The case at Xai-Xai. African Journal of Aquatic Science, 29(1), 113-116. Perry, C. T. (2003). Reef development at Inhaca Island, Mozambique: Coral communities and impacts of the 1999/2000 southern African floods. Ambio, 32(2), 134-139. Phongsuwan, N., Chankong, A., Yamarunpatthana, C., Chansang, H., Boonprakob, R., Petchkumnerd, P., . . . Bundit, O. A. (2013). Status and changing patterns on coral reefs in Thailand during the last two decades. Deep-Sea Research Part II: Topical Studies in Oceanography, 96, 19-24. Reyes-Bonilla, H., Carriquiry, J. D., Leyte-Morales, G. E., & Cupul-Magaña, A. L. (2002). Effects of the El Niño-Southern Oscillation and the anti-El Niño event (1997-1999) on coral reefs of the western coast of México. Coral Reefs, 21(4), 368-372. Ridgway, T., Inostroza, K., Synnot, L., Trapon, M., Twomey, L., & Westera, M. (2016). Temporal patterns of coral cover in the offshore Pilbara, Western Australia. Marine Biology, 163(9). Riegl, B. (2002). Effects of the 1996 and 1998 positive sea-surface temperature anomalies on corals, coral diseases and fish in the Arabian Gulf (Dubai, UAE). Marine Biology, 140(1), 29-40. Rioja-Nieto, R., Chiappa-Carrara, X., & Sheppard, C. (2012). Effects of hurricanes on the stability of reef-associated landscapes. Ciencias Marinas, 38(1), 47-55. Rogers, C. S., Gilnack, M., & Fitz Iii, H. C. (1983). Monitoring of coral reefs with linear transects: A study of storm damage. Journal of Experimental Marine Biology and Ecology, 66(3), 285-300. Rousseau, Y., Galzin, R., & Maréchal, J. P. (2010). Impact of hurricane Dean on coral reef benthic and fish structure of Martinique, French West Indies. Cybium, 34(3), 243-256. Russ, G. R., & Leahy, S. M. (2017). Rapid decline and decadal-scale recovery of corals and Chaetodon butterflyfish on Philippine coral reefs. Marine Biology, 164(1). Ruzicka, R. R., Colella, M. A., Porter, J. W., Morrison, J. M., Kidney, J. A., Brinkhuis, V., . . . Colee, J. (2013). Temporal changes in benthic assemblages on Florida Keys reefs 11 years after the 1997/1998 El Niño. Marine Ecology Progress Series, 489, 125-141. Sheppard, C. R. C. (1999). Coral decline and weather patterns over 20 years in the Chagos Archipelago, central Indian Ocean. Ambio, 28(6), 472-478. Shulman, M. J., & Robertson, D. R. (1996). Changes in the coral reefs of San Bias, Caribbean Panama: 1983 to 1990. Coral Reefs, 15(4), 231-236. Smith, T. B., Brandt, M. E., Calnan, J. M., Nemeth, R. S., Blondeau, J., Kadison, E., . . . Rothenberger, P. (2013). Convergent mortality responses of Caribbean coral species to seawater warming. Ecosphere, 4(7). Steneck, R. S., Arnold, S. N., Boenish, R., de León, R., Mumby, P. J., Rasher, D. B., & Wilson, M. W. (2019). Managing Recovery Resilience in Coral Reefs Against Climate-Induced Bleaching and Hurricanes: A 15 Year Case Study From Bonaire, Dutch Caribbean. Frontiers in Marine Science, 6(265). Stobart, B., Teleki, K., Buckley, R., Downing, N., & Callow, M. (2005). Coral recovery at Aldabra Atoll, Seychelles: Five years after the 1998 bleaching event. Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences, 363(1826), 251-255. Torda, G., Sambrook, K., Cross, P., Sato, Y., Bourne, D. G., Lukoschek, V., . . . Willis, B. L. (2018). Decadal erosion of coral assemblages by multiple disturbances in the Palm Islands, central Great Barrier Reef. Scientific Reports, 8(1). Trapon, M. L., Pratchett, M. S., & Penin, L. (2011). Comparative effects of different disturbances in coral reef habitats in Moorea, French Polynesia. Journal of Marine Biology, 2011. Tsounis, G., & Edmunds, P. J. (2017). Three decades of coral reef community dynamics in St. John, USVI: A contrast of scleractinians and octocorals. Ecosphere, 8(1). Van Woesik, R., De Vantier, L. M., & Glazebrook, J. S. (1995). Effects of Cyclone "Joy' on nearshore coral communities of the Great Barrier Reef. Marine Ecology Progress Series, 128(1-3), 261-270. Van Woesik, R., Sakai, K., Ganase, A., & Loya, Y. (2011). Revisiting the winners and the losers a decade after coral bleaching. Marine Ecology Progress Series, 434, 67-76. Vercelloni, J., Kayal, M., Chancerelle, Y., & Planes, S. (2019). Exposure, vulnerability, and resiliency of French Polynesian coral reefs to environmental disturbances. Scientific Reports, 9(1). Walsh, W. J. (1983). Stability of a coral reef fish community following a catastrophic storm. Coral Reefs, 2(1), 49-63. Wilkinson, C. (2004). Status of coral reefs of the world: 2004 (Vol. 2). Queensland, Australia: Global Coral Reef Monitoring Network. Wilkinson, C. R., & Souter, D. (2008). Status of Caribbean coral reefs after bleaching and hurricanes in 2005. Wismer, S., Tebbett, S. B., Streit, R. P., & Bellwood, D. R. (2019). Spatial mismatch in fish and coral loss following 2016 mass coral bleaching. Science of the Total Environment, 650, 1487-1498. Woolsey, E., Bainbridge, S. J., Kingsford, M. J., & Byrne, M. (2012). Impacts of cyclone Hamish at One Tree Reef: Integrating environmental and benthic habitat data. Marine Biology, 159(4), 793-803. Aim: Understand the interplay between resistance and recovery on coral reefs, and investigate dependence on pre- and post-disturbance states, to inform generalisable reef resilience theory across large spatial and temporal scales. Location: Tropical coral reefs globally. Time period: 1966 to 2017. Major taxa studied: Scleratinian hard corals. Methods: We conducted a literature search to compile a global dataset of total coral cover before and after acute storms, temperature stress, and coastal runoff from flooding events. We used meta-regression to identify variables that explained significant variation in disturbance impact, including disturbance type, year, depth, and pre-disturbance coral cover. We further investigated the influence of these same variables, as well as post-disturbance coral cover and disturbance impact, on recovery rate. We examined the shape of recovery, assigning qualitatively distinct, ecologically relevant, population growth trajectories: linear, logistic, logarithmic (decelerating), and a second-order quadratic (accelerating). Results: We analysed 427 disturbance impacts and 117 recovery trajectories. Accelerating and logistic were the most common recovery shapes, underscoring non-linearities and recovery lags. A complex but meaningful relationship between the state of a reef pre- and post-disturbance, disturbance impact magnitude, and recovery rate was identified. Fastest recovery rates were predicted for intermediate to large disturbance impacts, but a decline in this rate was predicted when more than ~75% of pre-disturbance cover was lost. We identified a shifting baseline, with declines in both pre-and post-disturbance coral cover over the 50 year study period. Main conclusions: We breakdown the complexities of coral resilience, showing interplay between resistance and recovery, as well as dependence on both pre- and post-disturbance states, alongside documenting a chronic decline in these states. This has implications for predicting coral reef futures and implementing actions to enhance resilience. The dataset provides a summary of all studies included in the analysis and the key statistics obtained from the studies and used in the analyses for the manuscript entitled "Coral reef state influences resilience to acute climate-mediated disturbances" as published in Global Ecology and Biogeography. The dataset includes details about the publication, spatial identifiers (e.g. realm, province, ecoregion) unique site code, information on the disturbance type and timing, the pre-and post-disturbance coral cover, the 5-year annual recovery rate, the recovery shape and recovery completeness classifications. Please see details Methods in the journal article "Coral reef state influences resilience to acute climate-mediated disturbances" as published in Global Ecology and Biogeography.
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2018Embargo end date: 10 Jan 2019Publisher:Dryad Pang, Rich; Van Breugel, Floris; Dickinson, Michael; Riffell, Jeffrey A.; Fairhall, Adrienne;doi: 10.5061/dryad.n0b8m
Flight trajectories of fruit flies and mosquitoes in a wind tunnel.This data file is a MySQL database file which must be uploaded to a MySQL database management system (DBMS) (e.g., via the MAMP installation: http://localhost:8888/MAMP/?language=English, as was used in the associated manuscript). Once you have installed a MySQL DBMS on your machine, make a new database called “wind_tunnel_db”. To populate this database using the data file, first download all of the data files and join them together using: cat wind_tunnel_db_* > wind_tunnel_db.sql Then run the following command to populate the wind_tunnel_db MySQL database with the result. /path/to/mysql -uroot -proot wind_tunnel_db < /path/to/wind_tunnel_db.sql replacing the paths and username/passwords as appropriate. It will take several minutes since it is a large file. The database contains several tables, which are mostly self explanatory. The key tables of interest are the “experiment” table, which lists the 4 experiments contained in this data set, the “timepoint” table, which contains the position, velocity, etc., of every fly/mosquito at every measured time point, and the “trajectory” table, which indicates which set of time points correspond to which individual trajectories. Other useful tables that have been pre-populated are the “crossing” table, which specifies trajectory segments corresponding to each plume crossing, and the “crossing_group” table, which groups sets of crossings together according to experiment and crossing identification criteria. The code that interacts with this database and recreates the figures in the associated manuscript is contained at https://github.com/rkp8000/wind_tunnel.wind_tunnel_db_aaPart 2wind_tunnel_db_abPart 3wind_tunnel_db_acPart 4wind_tunnel_db_adPart 5wind_tunnel_db_aePart 6wind_tunnel_db_afPart 7wind_tunnel_db_agPart 8wind_tunnel_db_ahPart 9wind_tunnel_db_aiInfotaxis databaseBase database for running infotaxis simulations. To see how to prepare and populate this database with simulated trajectory data, see the file _paper_auxiliary_code in the GitHub repository http://github.com/rkp8000/wind_tunnel.infotaxis_db.sql Natural decision-making often involves extended decision sequences in response to variable stimuli with complex structure. As an example, many animals follow odor plumes to locate food sources or mates, but turbulence breaks up the advected odor signal into intermittent filaments and puffs. This scenario provides an opportunity to ask how animals use sparse, instantaneous, and stochastic signal encounters to generate goal-oriented behavioral sequences. Here we examined the trajectories of flying fruit flies (Drosophila melanogaster) and mosquitoes (Aedes aegypti) navigating in controlled plumes of attractive odorants. While it is known that mean odor-triggered flight responses are dominated by upwind turns, individual responses are highly variable. We asked whether deviations from mean responses depended on specific features of odor encounters, and found that odor-triggered turns were slightly but significantly modulated by two features of odor encounters. First, encounters with higher concentrations triggered stronger upwind turns. Second, encounters occurring later in a sequence triggered weaker upwind turns. To contextualize the latter history dependence theoretically, we examined trajectories simulated from three normative tracking strategies. We found that neither a purely reactive strategy nor a strategy in which the tracker learned the plume centerline over time captured the observed history dependence. In contrast, “infotaxis”, in which flight decisions maximized expected information gain about source location, exhibited a history dependence aligned in sign with the data, though much larger in magnitude. These findings suggest that while true plume tracking is dominated by a reactive odor response it might also involve a history-dependent modulation of responses consistent with the accumulation of information about a source over multi-encounter timescales. This suggests that short-term memory processes modulating decision sequences may play a role in natural plume tracking.
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2023Publisher:Zenodo Authors: Markus Stoffel; Daniel G. Trappmann; Mattias I. Coullie; Juan A. Ballesteros-Cánovas; +1 AuthorsMarkus Stoffel; Daniel G. Trappmann; Mattias I. Coullie; Juan A. Ballesteros-Cánovas; Christophe Corona;This readme file provides all data and R codes used to perform the analyses presented in Figs. 2-4 of the main text and Supplementary Information Figures S1-S2-S3. FIGURE 2 - Seasonally_dated_GDs.txt: Contains information on the timing (Season) of rockfall (GD) in a given tree (Id) and a given year (yr) over the past 100 years. Inv refers to the operators which analyzed growth disturbances in the tree-ring series. Lat / Long refers to the position of the tree in CH1903/ Swiss Grid projection. Intensity (1-4) refers to (1), intermediate (2) and strong (3) GD. Intensity 4 was attributed to injuries (I). Only the 408 GD rated 3 (strong TRD) and 4 (injuries) were used in Fig. 2. Acronyms used for Response_type read as follows: TRD: Tangential rows of traumatic resin ducts; I: Injuries. Acronyms used for Season refer to Dormancy (1_D), early (2_EE), middle (3_ME) and late (4_LE) earlywood, whereas a GD found in the latewood was attributed to either the early (5_EL) or late (6_LL) latewood. - Trends_in_seasonality_R1.R: The data contained in "Seasonally_dated_GDs" were processed with the R script "Trends_in_Seasonality.R". This seasonal trend analysis code is inspired by work published by Schlögl et al. (2021; https://doi.org/10.1016/j.crm.2021.100294) and Heiser et al. (2022; https://doi.org/10.1029/2011JF002262). FIGURE 3-4-S1 - Tasch_GD.txt: Contains the raw data on rockfall impacts (GD) in a given year (yr) as found in all trees available in that same year (Sample_depth) as well as the cumulated diameter at breast height (cumulated_DBH) of all trees present in that same year. - Rockfall_frequency_climate.R: The data contained in "Tasch_GD.txt" were processed with the R script "Rockfall_frequency_climate.R". - The temperature (Imfeld23_tmp.txt) and precipitation (Imfeld23_prc.txt) data used in Fig. 3 are from the Imfeld et al. 2023 (10.5194/cp-19-703-2023) gridded dataset (1x1 km lat/long) and were extracted at the grid point centered on the Täschgufer site. - The script set with temperature series enables to compute Fig. 4 (l.149:216) and Fig. 3 (l. 216:330); the script set with precipitation series enables to compute Fig. S1 FIGURE S2 - Tasch_GD.txt: Contains the raw data on rockfall impacts (GD) at the Täschgufer site in a given year (yr) as found in all trees available in that same year (Sample_depth) as well as the cumulated diameter at breast height (cumulated_DBH) of all trees present in that same year. - Rockfall_frequency_borehole.R: is adapted from "Rockfall_frequency_climate.R" to work with the borehole dates. - Corvatsch0_6R1: Contains the Corvatsch borehole temperature series (2000-2020, 0.6m depth) (Hoelzle, M. et al. https://doi.org/10.5194/essd-14-1531-2022, 2022). FIGURE S3 - Plattje_GD.txt: Contains the raw data on rockfall impacts (GD) at the Plattje site in a given year (yr) as found all trees available in that same year (Sample_depth) as well as the cumulated diameter at breast height (cumulated_DBH) of all trees present in that same year. - - Rockfall_frequency_climate_Plattje.R: The data contained in "Plattje_GD.txt" were processed with the R script "Rockfall_frequency_climate_Plattje.R". - The temperature (Imfeld23_tmp_Plattje.txt) and precipitation (Imfeld23_prc_Plattje.txt) data used in Fig. 3 are from Imfeld et al. 2023 (10.5194/cp-19-703-2023) gridded dataset (1x1 km lat/long) and were extracted at the grid point centered on the Plattje site.
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You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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