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# 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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Mass coral bleaching due to unprecedented marine heatwave in Papahānaumokuākea Marine National Monument (Northwestern Hawaiian Islands). PLoS ONE, 12(9). Crabbe, M. J. C. (2014). Evidence of initial coral community recovery at Discovery Bay on Jamaica’s north coast. Revista de Biologia Tropical, 62, 137-140. Crosbie, A. J., Bridge, T. C., Jones, G., & Baird, A. H. (2019). Response of reef corals and fish at Osprey Reef to a thermal anomaly across a 30 m depth gradient. Marine Ecology Progress Series, 622, 93-102. Darling, E. S., McClanahan, T. R., & Côté, I. M. (2010). Combined effects of two stressors on Kenyan coral reefs are additive or antagonistic, not synergistic. Conservation Letters, 3(2), 122-130. De Bakker, D. M., Meesters, E. H., Bak, R. P. M., Nieuwland, G., & Van Duyl, F. C. (2016). Long-term Shifts in Coral Communities On Shallow to Deep Reef Slopes of Curaçao and Bonaire: Are There Any Winners? Frontiers in Marine Science, 3(247). Depczynski, M., Gilmour, J. 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(2016). 27 years of benthic and coral community dynamics on turbid, highly urbanised reefs off Singapore. Scientific Reports, 6. Guillemot, N., Chabanet, P., & Le Pape, O. (2010). Cyclone effects on coral reef habitats in New Caledonia (South Pacific). Coral Reefs, 29(2), 445-453. Guzmán, H. M., & Cortés, J. (2001). Changes in reef community structure after fifteen years of natural disturbances in the Eastern Pacific (Costa Rica). Bulletin of Marine Science, 69(1), 133-149. Guzman, H. M., Cortes, J., Richmond, R. H., & Glynn, P. W. (1987). Effects of "El Nino - Southern oscillation' 1982/83 in the coral reefs at Isla del Cano, Costa Rica. Revista de Biologia Tropical, 35(2), 325-332. Haapkylä, J., Melbourne-Thomas, J., Flavell, M., & Willis, B. L. (2013). Disease outbreaks, bleaching and a cyclone drive changes in coral assemblages on an inshore reef of the Great Barrier Reef. Coral Reefs, 32(3), 815-824. Hagan, A., & Spencer, T. (2008). 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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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.

This dataset contains time series of reservoir releases (including any spills), evaporation loss, and rule curves for the Pong and Bhakra reservoirs, India. {"references": ["https://doi.org/10.3390/w11071413", "https://doi.org/10.1016/j.scitotenv.2019.06.021"]}

Daily rainfall is measured as the total (mm) over the 24-hour period 0900 to 0900 GMT. It includes all precipitation - snow, rain, mist and fog. Rainfall was first recorded at Rothamsted in March 1853, using a copper funnel rain gauge (5 inch / 12.7 cm diameter) and measured using a graduated cylinder. Since 2004 it has been measured using an electronic tipping bucket rain gauge (10 inch / 25.4cm diameter), ARG100, calibrated to tip at 0.2mm (which has since become the minimum amount of rain that can be recorded). The rain gauge is placed within a 30cm deep 1.5m radius turf wall, retained by brick, to reduce wind eddies that may potentially blow rain out of the gauges. Data were collected daily manually until 2004 and since then by Automatic Weather Station using a standard protocol. There are differences in the capture rate between the two gauges, see Rainfall for further information. The monthly summary data contained in this spreadsheet are derived from daily data measured at Rothamsted Meteorological Station, Harpenden. Total monthly data is determined from daily data using Genstat 19th Edition. Verification includes checks for instrument errors, for missing data and outliers. The original raw daily data is available, after registering, from the e-RA database. Please contact the e-RA Curators for an access password and further details. This dataset represents the mean monthly rainfall recorded at Rothamsted from October 1985 - September 2017 and is derived from continuous daily records measured at the site. Location: Rothamsted Meteorological Station, Harpenden, Hertfordshire, England 51.82 N 0.37 W 128 m asl.

AbstractThe integration of power plants and desalination systems has attracted increasing attention over the past few years as an effective solution to tackle sustainable development and climate change issues. In this light, this paper introduces a novel modelling and optimization approach for a combined-cycle power plant (CCPP) integrated with reverse osmosis (RO) and multi-effect distillation (MED) desalination systems. The integrated CCPP and RO–MED desalination system is thermodynamically modelled utilizing MATLAB and EES software environments, and the results are validated via Thermoflex software simulations. Comprehensive energy, exergic, exergoeconomic, and exergoenvironmental (4E) analyses are performed to assess the performance of the integrated system. Furthermore, a new multi-objective water cycle algorithm (MOWCA) is implemented to optimize the main performance parameters of the integrated system. Finally, a real-world case study is performed based on Iran's Shahid Salimi Neka power plant. The results reveal that the system exergy efficiency is increased from 8.4 to 51.1% through the proposed MOWCA approach, and the energy and freshwater costs are reduced by 8.4% and 29.4%, respectively. The latter results correspond to an environmental impact reduction of 14.2% and 33.5%. Hence, the objective functions are improved from all exergic, exergoeconomic, and exergoenvironmental perspectives, proving the approach to be a valuable tool towards implementing more sustainable combined power plants and desalination systems.

Survival and growth of woody species in the Mediterranean are mainly restricted by water availability. We tested the hypothesis that Mediterranean species acclimate their xylem vulnerability and osmotic potential along a precipitation gradient. We studied five predominant co-occurring Mediterranean species; Quercus calliprinos, Pistacia palaestina, Pistacia lentiscus, Rhamnus lycioides, and Phillyrea latifolia, over two summers at three sites. The driest of the sites is the distribution edge for all the five species. We measured key hydraulic and osmotic traits related to drought resistance, including resistance to embolism (Ψ50) and the seasonal dynamics of water and osmotic potentials. The leaf water potentials (Ψ1) of all species declined significantly along the summer, reaching significantly lower Ψl at the end of summer in the drier sites. Surprisingly, we did not find plasticity along the drought gradient in Ψ50 or osmotic potentials. This resulted in much narrower hydraulic safety margins (HSM) in the drier sites, where some species experienced significant embolism. Our analysis indicates that reduction in HSM to null values put Mediterranean species in embolism risk as they approach their hydraulic limit near the geographic dry edge of their distribution. The PLC curves and resistance to embolism were measured using the Cavitron. The pre-dawn and midday water potentials were measured using a pressure bomb. The C13 was measured with a 13C cavity ring-down analyzer. The osmotic potential was measured using an osmometer. All methods are described in Alon et al., Acclimation limits for embolism resistance and osmotic adjustment accompany the geographic dry edge of Mediterranean species. 2023. Functional Ecology Excel

1. Aphids are abundant in natural and managed vegetation, supporting a diverse community of organisms and causing damage to agricultural crops. Due to a changing climate, periods of drought are anticipated to increase, and the potential consequences of this for aphid-plant interactions are unclear. 2. Using a meta-analysis and synthesis approach, we aimed to advance understanding of how increased drought incidence will affect this ecologically and economically important insect group, and to characterise any potential underlying mechanisms. We used qualitative and quantitative synthesis techniques to determine whether drought stress has a negative, positive, or null effect on aphid fitness and examined these effects in relation to 1) aphid biology, 2) geographical region, 3) host plant biology. 3. Across all studies, aphid fitness is typically reduced under drought. Subgroup analysis detected no difference in relation to aphid biology, geographical region, or the aphid-plant combination, indicating the negative effect of drought on aphids is potentially universal. Furthermore, drought stress had a negative impact on plant vigour and increased plant concentrations of defensive chemicals, suggesting the observed response of aphids is associated with reduced plant vigour and increased chemical defence in drought-stressed plants. 4. We propose a conceptual model to predict drought effects on aphid fitness in relation to plant vigour and defence to stimulate further research. Please check the ReadMe for an explanation of the values included in the dataset. Please note that n/a values are included in the Global_Dataset tab for plant meta-analysis data (_Plant_Vigour, _Plant_Defence, and _Plant_Nutrition), these indicate studies that did not report these parameters. Data was collected and curated using standard systematic literature synthesis approaches. The effect size (Hedges' g) reported in the dataset was calculated from extracted means and standard deviations.

Optimisation results for the lowest lifetime cost system consisting of solar photovoltaic (PV), hybrid photovoltaic-thermal (PV-T) and solar-thermal collectors alongside battery and hot-water storage systems for meeting the electrical and thermal (hot-water) needs of three multi-effect distillation (MED) plants. The updated results are from optimisations runs carried out in response to peer-review comments.

Water resources index W quantifies the potential dependence of the world's lowland areas on water resources originating in mountain areas upstream. The data cover the timeframe from the 1960s (1961–1970) to the 2040s (2041–2050) in decadal steps. Data for projections from the 2010s onwards are available for three scenario pathways (SSP1-RCP4.5, SSP2-RCP6.0, SSP3-RCP6.0) and show median results from 5 CMIP5 GCMs (GFDL-ESM2M, HadGEM2-ES, IPSL-CM5A-LR, MIROC-ESM-CHEM, NorESM1‑M). The files are GeoTIFF formatted and in a regular raster of 5’×5’ (arc minutes in WGS 1984 coordinate system) The values of W can be classified using the following ranges: W ≤ -2 → Essential but vastly insufficient -2 < W < -1 → Essential but insufficient -1 ≤ W < 0 → Essential and sufficient W = 0 → No surplus from mountains 0 < W ≤ 1 → Supportive 1 < W < 2 → Minor W ≥ 2 → Negligible The values of W are rounded to four decimal places and limited to a range of -1110 to 9998. Values falling outside of that range are set to the nearest limit. he following flag values apply to W: -5555 indicates that there is no water balance surplus from the mountain area upstream, but a lowland water balance surplus; -6666 indicates that there is no water balance surplus from the mountain area upstream, and a lowland water balance deficit. Mountain areas and oceans are NODATA, large ice shields are omitted (Greenland: NODATA, Antarctica: not covered in extent). Mountain areas provide disproportionally high runoff in many parts of the world, and here we quantify for the first time their importance for water resources and food production from the viewpoint of the lowland areas downstream. The dataset maps the degree to which lowland areas potentially depend on runoff contributions from mountain areas (39% of land mass) between the 1960s and the 2040s.