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As part of global efforts to reduce dependence on carbon-based energy sources there has been a rapid increase in the installation of renewable energy devices. The installation and operation of these devices can result in conflicts with wildlife. In the marine environment, mammals may avoid wind farms that are under construction or operating. Such avoidance may lead to more time spent travelling or displacement from key habitats. A paucity of data on at-sea movements of marine mammals around wind farms limits our understanding of the nature of their potential impacts. Here, we present the results of a telemetry study on harbour seals Phoca vitulina in The Wash, south-east England, an area where wind farms are being constructed using impact pile driving. We investigated whether seals avoid wind farms during operation, construction in its entirety, or during piling activity. The study was carried out using historical telemetry data collected prior to any wind farm development and telemetry data collected in 2012 during the construction of one wind farm and the operation of another. Within an operational wind farm, there was a close-to-significant increase in seal usage compared to prior to wind farm development. However, the wind farm was at the edge of a large area of increased usage, so the presence of the wind farm was unlikely to be the cause. There was no significant displacement during construction as a whole. However, during piling, seal usage (abundance) was significantly reduced up to 25 km from the piling activity; within 25 km of the centre of the wind farm, there was a 19 to 83% (95% confidence intervals) decrease in usage compared to during breaks in piling, equating to a mean estimated displacement of 440 individuals. This amounts to significant displacement starting from predicted received levels of between 166 and 178 dB re 1 μPa(p-p). Displacement was limited to piling activity; within 2 h of cessation of pile driving, seals were distributed as per the non-piling scenario. Synthesis and applications. Our spatial and temporal quantification of avoidance of wind farms by harbour seals is critical to reduce uncertainty and increase robustness in environmental impact assessments of future developments. Specifically, the results will allow policymakers to produce industry guidance on the likelihood of displacement of seals in response to pile driving; the relationship between sound levels and avoidance rates; and the duration of any avoidance, thus allowing far more accurate environmental assessments to be carried out during the consenting process. Further, our results can be used to inform mitigation strategies in terms of both the sound levels likely to cause displacement and what temporal patterns of piling would minimize the magnitude of the energetic impacts of displacement. Wash_diagWash_diag.xlsx is the historic location data (pre windfarm construction) for the 19 individuals used in the analysis described in Russell et al.

This research evaluates the current carbon footprint of vertical farming systems by comparing the impact of one kilogram of butterhead lettuce produced in an operational vertical farm to that of conventional open-field farming (OF), soil-based greenhouse cultivation (GH(s)) and hydroponic greenhouse cultivation (GH(h)) in the Netherlands. A typical farm is defined for OF, GH(s) and GH(h) in the Netherlands, based on existing databases. It is not yet possible to define a typical vertical farm (VF) due to the breadth of approaches. Therefore, an operational vertical farm was used as a case study. Within the dataset the baseline activity data has been collected within the tabs ‘OF’, ‘GH(s)’, GH(h) and ‘VF’. The carbon footprint of each case study was calculated by accounting for all the GHG emissions from activities within the system boundaries, from cradle-to-grave, for the life cycle of both the crop and the farm. These GHG emissions were calculated as follows: CO₂-eq = activity data x EF, where CO2-eq is the carbon footprint of the activity in kg CO2-eq, and EF is the emission factor of the activity in kg CO₂-eq per unit of the activity data, assessed by referring to the IPCC GWP100a characterisation method in SimaPro 9.0.0, which is based on the Ecoinvent 3.6 database. Tab ‘EF’ provides an overview of the emissions factor sources used for activities within the study. Country-specific emission factors for the Netherlands were used for natural gas and electricity consumption to reflect the correct energy mix. By combining the collected activity data with the EFs, the carbon footprints of each farming system were calculated within the tabs ‘FIG04’ and ‘FIG05’. Three scenarios were created to improve the comparability of the baseline data as well as present potential carbon savings as a result of transitioning to renewable energy, which included: the lost carbon sequestration potential as a result of land-use change (FIG06), assuming identical sales packaging for all farming systems (FIG07, FIG08, FIG09), and a transition to renewable energy (FIG10). These scenarios, when considered collectively, greatly reduced the disparity between the carbon footprints of the three farming systems (FIG11 and FIG12). Electricity use represented the largest share in the carbon fooptrint of both baseline and alternative scenario, therefore, the electricity consumption of the VF was compared to that of other VF from literature in the tabs ‘FIG13’ and ‘FIG14’.

Many species are too slow to track their poleward moving climate niche under global warming. Pesticide exposure may contribute to this by reducing population growth and impairing flight ability. Moreover, edge populations at the moving range front may be more vulnerable to pesticides because of the rapid evolution of traits to enhance their rate of spread that shunt energy away from detoxification and repair. We exposed replicated edge and core populations of the poleward moving damselfly Coenagrion scitulum to the pesticide esfenvalerate at low and high densities. Exposure to esfenvalerate had strong negative effects on survival, growth rate and development time in the larval stage and negatively affected flight-related adult traits (mass at emergence, flight muscle mass and fat content) across metamorphosis. Pesticide effects did not differ between edge and core populations, except that at the high concentration the pesticide-induced mortality was 17% stronger in edge populations. Pesticide exposure may therefore slow down the range expansion by lowering population growth rates, especially because edge populations suffered a higher mortality, and by negatively affecting dispersal ability by impairing flight-related traits. These results emphasize the need for direct conservation efforts toward leading-edge populations for facilitating future range shifts under global warming. MAIN DATAEVA-2015-167-OA DATA.xlsSUPPLEMENTARY DATA FOR APPENDICES (BIOTIC AND ABIOTIC PARAMETERS)EVA-2015-167-OA DATA FOR APPENDICES (BIOTIC AND ABIOTIC PARAMETERS).xls

First, this data complies CO2 emissions, final energy consumption, GDP, share of zero emitting electricity for Annex B countries of Kyoto Protocol and east state in U.S. Second, this data also complies all the CDM projects and monitoring reports until the end of the first commitment period of the Kyoto Protocol. The all the projects complies the result of additonality assessment.

The dataset covers biotic and abiotic data from the aquatic habitat of a population of the sediment-rooted macrophyte Myriophyllum spicatum in the temperate climate region (The Netherlands). The growth of M. spicatum was monitored in 0.2025 m2 plant baskets installed in an experimental ditch. Parameters monitored included biomass (fresh and dry weight), shoot length, seasonal short-term growth rates of shoots, relevant environmental parameters and weather data. This dataset includes the 2-year experimental biotic (macrophyte biomass and growth data) and environmental data (water quality data, sediment data). A second file includes the statistical data. A third file includes the weather data.

Figure 1data_Exp 2Figure 1 data: Condition of experimental seedlings in hummocks with contrasting shrub density and tree canopy in Experiment 2: No Trees - Low Shrub biomass (NTLS), No Trees - High Shrub biomass (NTHS), Present Trees - Low Shrub biomass (PTLS) and Present Trees - High shrub biomass (PTHS) during the warmest growing season (2011) and at the end of the experiment (2013). Seedling condition was defined as: healthy (< 50% of the needles turned yellow or brown) or unhealthy (> 50% of the needles turned yellow or brown). Seedlings were 1 month old at plantation time in the July 2010.Table 1_environmental conditions_Exp 1Table 1 data: Environmental conditions and vegetation characteristics in hummocks (circular and bands) and lawns for Experiment 1. Water table depth below surface is an average for the four growing seasons (2010-2013)Table 2_ photosynthesis data_Exp 1Table 2 photosynthesis data: Photosynthesis rates for experimental pine seedlings in hummocks (circular and bands) versus adjacent lawns for Experiment 1.Table 2_seedling responses_Exp 1Table 2 data: Responses of experimental pine seedlings in hummocks (circular and bands) versus adjacent lawns for Experiment 1 after 4 growing seasons. ST: Seeds inserted on top of moss; SB: Seeds inserted below moss; Small seedling (1 month old at plantation time); Large seedling (2 months old at plantation time). Emergence = % of planted seeds emerged after 1 year. Condition = % healthy seedlings. Stem growth corresponds to vertical stem growth for germinating (ST and SB) seedlings and new stem growth for older (small and large) seedlings.Table 3_regression seedling-environment_Exp 1Table 3 data for generalized linear models assessing the responses of experimental pine seedlings in hummocks (circular and bands) and adjacent lawns for Experiment 1 during the whole experimental period (2010-2013). ST: Seedlings from seeds inserted on top of moss; SB: Seedlings from seeds inserted below moss; Small seedling (1 month old at plantation time); Large seedling (2 months old at plantation time). Condition = % healthy seedlings. Growth = stem growth.Table 4_Environmental data_Exp 2Table 4: Environmental conditions in hummocks with contrasting shrub density and tree canopy in Experiment 2: No Trees - Low Shrub biomass (NTLS), No Trees - High Shrub biomass (NTHS), Present Trees - Low Shrub biomass (PTLS) and Present Trees - High shrub biomass (PTHS).Table 4 and Table S5a_seedling performance_Exp 2Table 4: Seedling performance in hummocks with contrasting shrub density and tree canopy in Experiment 2: No Trees - Low Shrub biomass (NTLS), No Trees - High Shrub biomass (NTHS), Present Trees - Low Shrub biomass (PTLS) and Present Trees - High shrub biomass (PTHS). Seedling emergence, condition and survival from seeds inserted below the moss (SB), and from small planted seedlings.Table S3_cox regression (survival analysis)_Exp 1Table S3: Data for Cox survival analysis for experimental pine seedlings in hummocks (circular and bands) versus adjacent lawns during 2010-2013. ST: Seedlings from seeds inserted on top of moss; SB: Seedlings from seeds inserted below moss; Small seedling (1 month old, 10 cm tall at plantation time); Large seedling (2 months old, 30 cm tall at plantation time).Table S4_ regression seedling-environment 2011_Exp 1Table S4: Data for generalized linear models assessing the responses of experimental pine seedlings in hummocks (circular and bands) and adjacent lawns for Experiment 1 in 2011. Small seedling (1 month old, 10 cm tall at plantation time); Large seedling (2 months old, 30 cm tall at plantation time). Condition = % healthy seedlings. Growth = stem growth. Boreal ecosystems are warming roughly twice as fast as the global average, resulting in woody expansion that could further speed up the climate warming. Boreal peatbogs are waterlogged systems that store more than 30% of the global soil carbon. Facilitative effects of shrubs and trees on the establishment of new individuals could increase tree cover with profound consequences for the structure and functioning of boreal peatbogs, carbon sequestration and climate. We conducted two field experiments in boreal peatbogs to assess the mechanisms that explain tree seedling recruitment and to estimate the strength of positive feedbacks between shrubs and trees. We planted seeds and seedlings of Pinus sylvestris in microsites with contrasting water-tables and woody cover and manipulated both shrub canopy and root competition. We monitored seedling emergence, growth and survival for up to four growing seasons and assessed how seedling responses related to abiotic and biotic conditions. We found that tree recruitment is more successful in drier topographical microsites with deeper water-tables. On these hummocks, shrubs have both positive and negative effects on tree seedling establishment. Shrub cover improved tree seedling condition, growth and survival during the warmest growing season. In turn, higher tree basal area correlates positively with soil nutrient availability, shrub biomass and abundance of tree juveniles. Synthesis. Our results suggest that shrubs facilitate tree colonization of peatbogs which further increases shrub growth. These facilitative effects seem to be stronger under warmer conditions suggesting that a higher frequency of warmer and dry summers may lead to stronger positive interactions between shrubs and trees that could eventually facilitate a shift from moss to tree-dominated systems.

All temperature measurements in well T96-012 from September 1996 to December 2011. Data presented in this spreadsheet were digitized from temperature-time graphs presented in AMEC, Environmental and Infrastructure (2012) and Water Management Consultants, Inc. (2001) (references below) by Joseph Batir. The exact date of temperature data collection was not completely apparent and digitization may have introduced minor date errors, so instead all temperature measurements are associated with the month data collection occurred. The digitized date of temperature collection is included, but should be used with caution. The second tab includes all temperature data plotted as temperature versus depth plots. Raw data sources: AMEC Environment and Infrastructure. (2012) Long-Term Permafrost and Groundwater Monitoring Program for the Tailing Impoundment Five-Year Permafrost and Groundwater Data Analysis 2007-2011, 479 pp. Water Management Consultants, Inc. (2001) Red Dog Mine Long-Term Permafrost and Groundwater Monitoring Plan for the Tailing Impoundment, 24 pp.