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Monitoring of plant succession in glacier forelands so far has been restricted to field sampling. In this study, in situ vegetation sampling along a chronosequence between Little Ice Age (LIA) maximum extent and the recent glacier terminus at Jamtalferner/Silvretta (ferner is a Tyrolian toponym for glacier) is compared to time series of the Normalized Difference Vegetation Index (NDVI) calculated from 13 Landsat scenes (1985-2016). The glacier terminus positions at 16 dates between the LIA maximum and 2015 were analysed from historical maps, orthophotos and LiDAR images and used for site age determination. We sampled plots of different time since deglaciation, from very recent to approx. 150 years: after 100 years, roughly 80% of the ground is covered by plants and ground cover did not increase essentially thereafter. Species number increases from 10-20 species on young sites to 40-50 species after 100 years. The NDVI increases for all plots between 1985 and 2016, from a mean of 0.11 for 1985-1991 to 0.2 in 2009 and 0.27 in 2016. For the plots deglaciated between 1 and about 150 years, the NDVI increases with the time of exposure. As the increase in ground cover is clearly reproduced by the NDVI (R² ground cover/NDVI 0.84) - even for sparsely vegetated areas -, we see a high potential of satellite-borne NDVI to perform regional characterizations of glacier forelands for hydrological, ecological and hazard management related applications. This data collection comprises the galcier outlines, NDVIs and chronosequencing locations with diversity and ground cover data.

Barnacles are dominant members of marine intertidal communities. Their success depends on firm attachment provided by their proteinaceous adhesive and protection imparted by their calcified shell plates. Little is known about how variations in the environment affect adhesion and shell formation processes in barnacles. Increased levels of atmospheric CO2 have led to a reduction in the pH of ocean waters (i.e., ocean acidification), a trend that is expected to continue into the future. Here, we assessed if a reduction in seawater pH, at levels predicted within the next 200 years, would alter physiology, adhesion, and shell formation in the cosmopolitan barnacle Amphibalanus (=Balanus) amphitrite. Juvenile barnacles, settled on silicone substrates, were exposed to one of three static levels of pHT, 8.01, 7.78, or 7.50, for 13 weeks. We found that barnacles were robust to reduced pH, with no effect of pH on physiological metrics (mortality, tissue mass, and presence of eggs). Likewise, adhesive properties (adhesion strength and adhesive plaque gross morphology) were not affected by reduced pH. Shell formation, however, was affected by seawater pH. Shell mass and base plate area were higher in barnacles exposed to reduced pH; barnacles grown at pHT 8.01 exhibited approximately 30% lower shell mass and 20% smaller base plate area as compared to those at pHT 7.50 or 7.78. Enhanced growth at reduced pH appears to be driven by the increased size of the calcite crystals that comprise the shell. Despite enhanced growth, mechanical properties of the base plate (but not the parietal plates) were compromised at the lowest pH level. Barnacle base plates at pHT 7.50 broke more easily and crack propagation, measured through microhardness testing, was significantly affected by seawater pH. Other shell metrics (plate thickness, relative crystallinity, and atomic disorder) were not affected by seawater pH. Hence, a reduction in pH resulted in larger barnacles but with base plates that would crack more readily. It is yet to be determined if such changes would alter the survival of A. amphitrite in the field, but changes in the abundance of this ecologically dominant species would undoubtedly affect the composition of biofouling communities. In order to allow full comparability with other ocean acidification data sets, the R package seacarb (Gattuso et al, 2019) was used to compute a complete and consistent set of carbonate system variables, as described by Nisumaa et al. (2010). In this dataset the original values were archived in addition with the recalculated parameters (see related PI). The date of carbonate chemistry calculation by seacarb is 2020-09-18.

The data shared in this package delivers the wildfire ignition probability and spreading capacity of vegetated surfaces in Romania following the method developed by Hysa and Baskaya (2019, https://doi.org/10.1007/s40808-018-0519-9). The model relies on remotely sensed free data that covers the time-lapse between 2015-2020. Geospatial information about sixteen criteria about anthropogenic, hydro-meteorological, geophysical, and fuel properties of Romanian territory are considered here. Raw data regarding each criterion is acquired for free from different online databases. The attribute table of the shared shapefile includes all inventory measurements per each criterion. It consist of 70410 point geometries in total representing 1km2 each, covering all vegetated surfaces of Romania. This data consist of a geospatial points layer (shp file), which deliver both the multi-criteria inventory records and the calculated wildfire ignition probability and wildfire spreading capacity (WIPI/WSCI) of the Romanian vegetated surfaces. The distance between points is 1km. The file consists of 70410 points in total, that overlap with the vegetated surfaces as derived from CORINE Land Cover data of 2018.

Surface solar radiation drives the water cycle and energy exchange on the earth's surface, and its diffuse component can promote carbon uptake in ecosystems by increasing the plant productivity. The accurate knowledge of their spatial distribution is of great importance to many studies and applications, such as the estimation of agricultural yield, carbon dynamics of terrestrial systems, site selection of solar power plants, as well as trends of regional climate changes. Therefore, we produce the hourly surface radiation datasets based on the hourly Multi-functional Transport Satellite (MTSAT) satellite imagery and the ground observations from the China Meteorology Administration (CMA) through deep learning techniques. The deep network is trained using training samples in 2008, and then utilized to generate the hourly radiation for other years. This dataset provides the gridded surface global and diffuse solar radiation in 2015 within 71.025°E - 141.025°E and 14.975°N - 59.975°N with an increment of 0.05°. Both the direct predicted hourly values and the integrated daily and monthly total values are available. The dataset should be useful for the analysis of the regional differences and temporal cycles of solar radiation in fine scales, and the impact of diffuse radiation on plant growth etc.

Poleward range extensions by warm-adapted sea urchins are switching temperate marine ecosystems from kelp-dominated to barren-dominated systems that favour the establishment of range-extending tropical fishes. Yet, such tropicalization may be buffered by ocean acidification, which reduces urchin grazing performance and the urchin barrens that tropical range-extending fishes prefer. Using ecosystems experiencing natural warming and acidification, we show that ocean acidification could buffer warming-facilitated tropicalization by reducing urchin populations (by 87%) and inhibiting the formation of barrens. This buffering effect of CO2 enrichment was observed at natural CO2 vents that are associated with a shift from a barren-dominated to a turf-dominated state, which we found is less favourable to tropical fishes. Together, these observations suggest that ocean acidification may buffer the tropicalization effect of ocean warming against urchin barren formation via multiple processes (fewer urchins and barrens) and consequently slow the increasing rate of tropicalization of temperate fish communities. In order to allow full comparability with other ocean acidification data sets, the R package seacarb (Gattuso et al, 2021) was used to compute a complete and consistent set of carbonate system variables, as described by Nisumaa et al. (2010). In this dataset the original values were archived in addition with the recalculated parameters (see related PI). The date of carbonate chemistry calculation by seacarb is 2021-07-26.

Marine prey and predators will respond to future climate through physiological and behavioral adjustments. However, our understanding of how such direct effects may shift the outcome of predator–prey interactions is still limited. Here, we investigate the effects of ocean warming and acidification on foraging behavior and biomass of a common prey (shrimps, Palaemon spp.) tested in large mesocosms harboring natural resources and habitats. Acidification did not alter foraging behavior in prey. Under warming, however, prey showed riskier behavior by foraging more actively and for longer time periods, even in the presence of a live predator. No effects of longer-term exposure to climate stressors were detected on prey biomass. Our findings suggest that ocean warming may increase the availability of some prey to predators via a behavioral pathway (i.e., increased risk-taking by prey), likely by elevating metabolic demand of prey species. In order to allow full comparability with other ocean acidification data sets, the R package seacarb (Gattuso et al, 2020) was used to compute a complete and consistent set of carbonate system variables, as described by Nisumaa et al. (2010). In this dataset the original values were archived in addition with the recalculated parameters (see related PI). The date of carbonate chemistry calculation by seacarb is 2020-12-08.

In order to allow full comparability with other ocean acidification data sets, the R package seacarb (Lavigne and Gattuso, 2011) was used to compute a complete and consistent set of carbonate system variables, as described by Nisumaa et al. (2010). In this dataset the original values were archived in addition with the recalculated parameters (see related PI). The date of carbonate chemistry calculation by seacarb is 2013-10-14.

At each station, seawater was collected for trace metals sampling at 20 m depth using a Teflon pump (Furon®) with a 40 m Teflon tube connected with a AcroPakTM 1500 capsule w/Supor Memb 0.8/0.2 μm filter. The pump was left to pump to rinse the inner hose and 1 L sample was collected in LDPE bottles (NALGENE) and stored at -20oC until the land-based laboratory analysis. The material was previously cleaned following the trace metals GEOTRACES protocol and the experiments were done in Class 100 clean laboratory or trace metal analysis (QUIMA- IOCAG TM lab).