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This is the dataset for our research on assessing CO2 emissions from Chinese inland waters, including streams, rivers, lakes and reservoirs. The dataset includes three parts, including Part 1: Lakes and Reservoirs_1980s, Part 2: CO2 Dataset_2010s, and Part 3: Water chemistry records. Detailed information on these data can be found from the 'README' text file.

Plot design and harvesting Twelve sampling plots (16 m × 16 m) in three P. deltoides plantations were established based on systematic random design. To minimize edge effects, surrounding rows were not considered during sampling. The age of the stands was 18-20 years old. In each sampling plot, the DBH (diameter at breast height 1.3 m above the ground) of the individual trees was measured with a caliper in two perpendicular directions and the mean DBH determined. Tree height was measured by Haglöf-Vertex IV hypsometer. Based on the DBH and height measurements, 10 DBH classes from 15 to 42 cm (3 cm intervals) were established. The value of each DBH class represented the central value (i.e., class 15 included all DBH from 12.5 to 17.5 cm). In each DBH class, one representative tree was selected and harvested for a total of 10 P. deltoides trees. Measurements of bark percentagesThe stems of harvested trees were marked and cut into 2 m-segments. The mid-length diameter of each segment was measured outside the bark in two perpendicular directions with a caliper to determine the mean diameter. A 5 cm-thick disc was cut from the middle of each segment. A total of 123 discs were obtained and brought to the laboratory. All the discs were arranged into 2-cm wide diameter classes. The value of each disc class represents the central value (i.e., class 20 included all discs whose diameters ranged from 19.5 to 20.5 cm). Bark was separated from the wood using a peeler knife for each disc. Fresh bark and wood were weighted separately, oven-dried at 80 °C until constant weight, and the oven-dry weight measured. The bark percentage of each disc was considered as bark percentage of a 2 m-segment for fresh and dry weight. Finally, the bark percentage of the whole stem in each DBH class was calculated by adding the 2 m-segments. Bark biomass as an energy source has a high economic value. Bark content variations and production helps recognize the potential of this bioenergy source spatially before harvesting. The percentage of fresh and dry bark in Populus deltoides grown under a monoculture system was examined in the temperate region of northern Iran. Diameter at breast height (DBH) and total height data were analyzed based on an initial inventory. Ten sample trees were felled, separated into 2 m-segments, and weighted in the field. A 5-cm-thick disc from each segment was extracted for determining fresh and dry bark percentages. These were statistically significantly different in disc diameter classes and decreased with increasing disc diameters. Bark percentage of the disc classes ranged from 21.8 to 24.4% in small-sized diameters to 8.1‒9.3% in large-sized diameters. The differences between fresh and dry bark percentages depended on water content variations. Allometric power equations were fitted to data of fresh and dry bark percentages and disc diameters as well as DBH. The values of R2 ranged from 0.89 to 0.90. In addition, allometric power equations provided the best fits for relationships between total stem dry biomass, dry bark biomass, and DBH, R2 = 0.986 and 0.979 for the total stem dry biomass and stem dry bark biomass, respectively. The allometric models can be used to estimate bark percentage and bark production of P. deltoides in segments and for the whole stem for a wide range of segment diameters (8‒44 cm) and DBH (15‒45 cm).

The atmosphere concentration of CO2 is steadily increasing and causing climate change. To achieve the Paris 1.5 or 2 oC target, negative emissions technologies must be deployed in addition to reducing carbon emissions. The ocean is a large carbon sink but the potential of marine primary producers to contribute to carbon neutrality remains unclear. Here we review the alterations to carbon capture and sequestration of marine primary producers (including traditional ‘blue carbon’ plants, microalgae, and macroalgae) in the Anthropocene, and, for the first time, assess and compare the potential of various marine primary producers to carbon neutrality and climate change mitigation via biogeoengineering approaches. The contributions of marine primary producers to carbon sequestration have been decreasing in the Anthropocene due to the decrease in biomass driven by direct anthropogenic activities and climate change. The potential of blue carbon plants (mangroves, saltmarshes, and seagrasses) is limited by the available areas for their revegetation. Microalgae appear to have a large potential due to their ubiquity but how to enhance their carbon sequestration efficiency is very complex and uncertain. On the other hand, macroalgae can play an essential role in mitigating climate change through extensive offshore cultivation due to higher carbon sequestration capacity and substantial available areas. This approach seems both technically and economically feasible due to the development of offshore aquaculture and a well-established market for macroalgal products. Synthesis and applications: This paper provides new insights and suggests promising directions for utilizing marine primary producers to achieve the Paris temperature target. We propose that macroalgae cultivation can play an essential role in attaining carbon neutrality and climate change mitigation, although its ecological impacts need to be assessed further. To calculate the parameters presented in Table 1, the relevant keywords "mangroves, salt marshes, macroalgae, microalgae, global area, net primary productivity, CO2 sequestration" were searched through the ISI Web of Science and Google Scholar in July 2021. Recent data published after 2010 were collected and used since area and productivity of plants change with decade. For data with limited availability, such as net primary productivity (NPP) of seagrasses and global area and NPP of wild macroalgae, data collection was extended back to 1980. Total NPP and CO2 sequestration for mangroves, salt marshes, seagrasses and wild macroalgae were obtained by the multiplication of area and NPP/CO2 sequestration density and subjected to error propagation analysis. Data were expressed as means ± standard error.

Seeds of 52 species of herbaceous plants typical from European grassland ecosystems were obtained from a commercial supplier (Planta naturalis). When species germinated in Petri dishes the seedlings were then transplanted to plastic pots (11 x 11 x 12 cm height, 1L volume). Pots were filled with a mixture of a potting substrate (Biolan Murumuld) and sand. Pots were randomly placed in the greenhouse of the University of Tartu, Estonia. Then, we established monocultures with seven individuals of a single species per pot which were grown under well-watered conditions. One month after transplanting the seedlings to the pots, a drought treatment was applied to half of the pots (five pots per species). The experiment was harvested in late July 2020, when the first individuals started flowering, after month-long drought treatment. Plant traits related to drought responses and resource use strategies were selected and measured for each species following established protocols. These included seven above- and belowground traits: Vegetative plant height (H, cm), Leaf Area (LA, mm2), Specific Leaf Area (SLA, mm2 mg-1), Leaf Dry Matter Content (LDMC, mg g-1), Specific Root Length (SRL, cm g-1), Average root Diameter (AvgD, mm), Root Dry Matter Content (RDMC, mg g-1). Before harvesting, we measured the plant height and collected one leaf per individual for three individuals per pot. Afterward, we collected the aboveground biomass and belowground biomass of all the individuals in each pot. Due to the difficulty in untangling the roots of the different individuals in a pot, root traits were estimated at the pot level. Roots were washed and a sample of finest roots (10-50mg) was collected. Leaves and fine roots were scanned at 300dpi and 600dpi, respectively, using an Epson perfection 3200 Photo scanner for leaves and Epson V700 Photo scanner for fine roots. After scanning, leaves and roots were oven-dried at 60°C for 72h. AvgD and root length were determined using WinRHIZO Pro 2015 (Regent Instruments Inc., Canada), and leaf area with ImageJ software. We averaged all traits values at the species level, attaining a single value for each trait in each treatment. The total aboveground biomass and total belowground biomass of each pot were oven-dried at 60°C for 72h and weighed. Drought is expected to increase in future climate scenarios. Although responses to drought of individual functional traits are relatively well-known, simultaneous changes across multiple traits in response to water scarcity remain poorly understood despite its importance to understand alternative strategies to resist drought. We grew 52 herbaceous species in monocultures under drought and control treatments and characterized the functional space using seven measured above- and belowground traits: plant height, leaf area, specific leaf area, leaf dry matter content, specific root length, average root diameter, and root dry matter content. Then, we estimated how each species occupied this space and the amount of functional space occupied in both treatments using trait probability density functions. We also estimated intraspecific trait variability (ITV) for each species as the dissimilarity in trait values between the individuals of each treatment. We then mapped drought resistance and ITV in the functional space using generalized additive models. The response of species to drought strongly depended on their traits, with species that invested more in root tissues and conserved small size being both more resistant to drought and having higher ITV. We also observed a significant trend of trait displacement towards less conservative strategies. However, these changes depended strongly on the trait values of species in the control treatment, with species with different traits having opposing responses to drought. These contrasting responses resulted in lower trait variability in the species pool in drought compared to control conditions. Our results suggest strong trait filtering acting on conservative species as well as the existence of an optimal part in the functional space to which species converge under drought. Our results show that changes in species trait-space occupancy are key to understand plant strategies to withstand drought, highlighting the importance of individual variation in response to environmental changes, and suggest that community-wide functional diversity and biomass productivity could decrease in a drier future. Knowing these shifts will help to anticipate changes in ecosystem functioning facing climate change. The complete dataset is in the file.

# 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. 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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.

Cities are progressively heightening their climate aspirations to curtail urban carbon emis- sions and establish a future where economies and communities can flourish within the Earth’s eco- logical limits. Consequently, numerous climate initiatives are being launched to control urban car- bon emissions, targeting various sectors, including transport, residential, agricultural, and energy. However, recent scientific literature underscores the disproportionate distribution of climate poli- cies. While cities in the Global North have witnessed several initiatives to combat climate change, cities in the Global South remain uncovered and highly vulnerable to climate hazards. To address this disparity, we employed the Balanced Iterative Reducing and Clustering using the Hierarchies (BRICH) algorithm to cluster cities from diverse geographical areas that exhibit comparable socio- economic profiles. This clustering strives to foster enhanced cooperation and collaboration among cities globally, with the goal of addressing climate change in a comprehensive manner. In summary, we identified similarities, pa􏰀erns, and clusters among peer cities, enabling mutual and generaliza- ble learning among worldwide peer-cities regarding urban climate policy exchange. This exchange occurs through three approaches: (i) inner-mutual learning, (ii) cross-mutual learning, and (iii) outer-mutual learning. Our findings mark a pivotal stride towards a􏰀aining worldwide climate ob- jectives through a shared responsibility approach. Furthermore, they provide preliminary insights into the implementation of “urban climate policy exchange” among peer cities on a global scale.

Comprehensive and reliable information on anthropogenic sources of greenhouse gas emissions is required to track progress towards keeping warming well below 2°C as agreed upon in the Paris Agreement. Here we provide a dataset on anthropogenic GHG emissions 1970-2019 with a broad country and sector coverage. We build the dataset from recent releases from the “Emissions Database for Global Atmospheric Research” (EDGAR) for CO2 emissions from fossil fuel combustion and industry (FFI), CH4 emissions, N2O emissions, and fluorinated gases and use a well-established fast-track method to extend this dataset from 2018 to 2019. We complement this with information on net CO2 emissions from land use, land-use change and forestry (LULUCF) from three available bookkeeping models.

Outputs from the Network Innovation Allowance project "Control REACT" (workstream 2), sponsored by National Grid Electricity System Operator (NGESO). This deposit contains underlying data used in this project. The R code (Rmarkdown) and html renders of these workbooks are available in a separate deposit linked below. See description there for further details. In order to run the R scripts, data and code must be arranged in the directory structure given in "Directory Structure.pdf". Wind, solar and net-demand data are derived from raw data made available by Elexon and Solar Sheffield via public APIs. See respective websites for details, our processed (aggregated and cleaned) versions of this data are shared here under a CC-BY license. Weather forecast data are derived from historic operational forecasts from the ECMWF HRES model and are shared under a CC-BY licence. For details on how these were processed please see references. {"references": ["J. Browell and M. Fasiolo, \"Probabilistic Forecasting of regional net-load with conditional extremes and gridded NWP\", IEEE Transactions on Smart Grid, vol. 12, no, 6, pp. 5011-5019, 2021", "C. Gilbert \"Topics in high dimensional energy forecasting\", J. Browell & D. McMillan, degree supervisors; Centre for Doctoral Training in Wind and Marine Energy Systems; Department of Electronic and Electrical Engineering Thesis [PhD] 2021"]}