Current analyses and predictions of spatially explicit patterns and processes in ecology most often rely on climate data interpolated from standardized weather stations. This interpolated climate data represents long-term average thermal conditions at coarse spatial resolutions only. Hence, many climate-forcing factors that operate at fine spatiotemporal resolutions are overlooked. This is particularly important in relation to effects of observation height (e.g. vegetation, snow and soil characteristics) and in habitats varying in their exposure to radiation, moisture and wind (e.g. topography, radiative forcing or cold-air pooling). Since organisms living close to the ground relate more strongly to these microclimatic conditions than to free-air temperatures, microclimatic ground and near-surface data are needed to provide realistic forecasts of the fate of such organisms under anthropogenic climate change, as well as of the functioning of the ecosystems they live in. To fill this critical gap, we highlight a call for temperature time series submissions to SoilTemp, a geospatial database initiative compiling soil and near-surface temperature data from all over the world. Currently, this database contains time series from 7,538 temperature sensors from 51 countries
Research in global change ecology relies heavily on global climatic grids derived from estimates of air temperature in open areas at around 2 m above the ground. These climatic grids thus fail to reflect conditions below vegetation canopies and near the ground surface, where critical ecosystem functions are controlled and most terrestrial species reside. Here we provide global maps of soil temperature and bioclimatic variables at a 1-km² resolution for 0-5 and 5-15 cm depth. These maps were created by calculating the difference (i.e., offset) between in-situ soil temperature measurements, based on time series from over 1200 1-km² pixels (summarized from 8500 unique temperature sensors) across all of the world's major terrestrial biomes, and coarse-grained air temperature estimates from ERA5-Land (an atmospheric reanalysis by the European Centre for Medium-Range Weather Forecasts). We show that mean annual soil temperature differs markedly from the corresponding 2 m gridded air temperature, by up to 10°C (mean = 3.0 ± 2.1°C), with substantial variation across biomes and seasons. Over the year, soils in cold and/or dry biomes are substantially warmer (3.6 ± 2.3°C warmer than gridded air temperature), whereas soils in warm and humid environments are on average slightly cooler (0.7 ± 2.3°C cooler). The observed substantial and biome-specific offsets underpin that the projected impacts of climate and climate change on biodiversity and ecosystem functioning are inaccurately assessed when air rather than soil temperature is used, especially in cold environments. The global soil-related bioclimatic variables provided here are an important step forward for any application in ecology and related disciplines. Nevertheless, we highlight the need to fill remaining global gaps by collecting more in-situ measurements of microclimate conditions to further enhance the spatiotemporal resolution of global soil temperature products for ecological applications.
Abstract. Climate warming is expected to induce treelines to advance to higher elevations. Empirical studies in diverse mountain ranges, however, give evidence of both advancing alpine treelines and rather insignificant responses. The inconsistency of findings suggests distinct differences in the sensitivity of global treelines to recent climate change. It is still unclear where Himalayan treeline ecotones are located along the response gradient from rapid dynamics to apparently complete inertia. This paper reviews the current state of knowledge regarding sensitivity and response of Himalayan treelines to climate warming, based on extensive field observations, published results in the widely scattered literature, and novel data from ongoing research of the present authors.Several sensitivity indicators such as treeline type, treeline form, seed-based regeneration, and growth patterns are evaluated. Since most Himalayan treelines are anthropogenically depressed, observed advances are largely the result of land use change. Near-natural treelines are usually krummholz treelines, which are relatively unresponsive to climate change. Nevertheless, intense recruitment of treeline trees suggests a great potential for future treeline advance. Competitive abilities of seedlings within krummholz thickets and dwarf scrub heaths will be a major source of variation in treeline dynamics. Tree growth-climate relationships show mature treeline trees to be responsive to temperature change, in particular in winter and pre-monsoon seasons. High pre-monsoon temperature trends will most likely drive tree growth performance in the western and central Himalaya. Ecological niche modelling suggests that bioclimatic conditions for a range expansion of treeline trees will be created during coming decades.
Roadsides are major pathways of plant invasions in mountain regions. However, the increasing importance of tourism may also turn hiking trails into conduits of non-native plant spread to remote mountain landscapes. Here, we evaluated the importance of such trails for plant invasion in five protected mountain areas of southern central Chile. We therefore sampled native and non-native species along 17 trails and in the adjacent undisturbed vegetation. We analyzed whether the number and cover of non-native species in local plant assemblages is related to distance to trail and a number of additional variables that characterize the abiotic and biotic environment as well as the usage of the trail. We found that non-native species at higher elevations are a subset of the lowland source pool and that their number and cover decreases with increasing elevation and with distance to trails, although this latter variable only explained 4-8% of the variation in the data. In addition, non-native richness and cover were positively correlated with signs of livestock presence but negatively with the presence of intact forest vegetation. These results suggest that, at least in the region studied, hiking trails have indeed fostered non-native species spread to higher elevations, although less efficiently than Co-last authors: Aníbal Pauchard and Stefan Dullinger.
Research in environmental science relies heavily on global climatic grids derived from estimates of air temperature at around 2 meter above ground1-3. These climatic grids however fail to reflect conditions near and below the soil surface, where critical ecosystem functions such as soil carbon storage are controlled and most biodiversity resides4-8. By using soil temperature time series from over 8500 locations across all of the world’s terrestrial biomes4, we derived global maps of soil temperature-related variables at 1 km resolution for the 0–5 and 5–15 cm depth horizons. Based on these maps, we show that mean annual soil temperature differs markedly from the corresponding 2 m gridded air temperature, by up to 10°C, with substantial variation across biomes and seasons. Soils in cold and/or dry biomes are annually substantially warmer (3.6°C ± 2.3°C) than gridded air temperature, whereas soils in warm and humid environments are slightly cooler (0.7 ± 2.3°C). As a result, annual soil temperature varies less (by 17%) across the globe than air temperature. The effect of macroclimatic conditions on the difference between soil and air temperature highlights the importance of considering that macroclimate warming may not result in the same level of soil temperature warming. Similarly, changes in precipitation could alter the relationship between soil and air temperature, with implications for soil-atmosphere feedbacks9. Our results underpin that the impacts of climate and climate change on biodiversity and ecosystem functioning are inaccurately assessed when air rather than soil temperature is used, especially in cold environments.
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