Climate warming is predicted to affect temperate forests severely, but the response of fine roots, key to plant nutrition, water uptake, soil carbon, and nutrient cycling is unclear. Understanding how fine roots will respond to increasing temperature is a prerequisite for predicting the functioning of forests in a warmer climate. We studied the response of fine roots and their ectomycorrhizal (EcM) fungal and root‐associated bacterial communities to soil warming by 4°C in a mixed spruce‐beech forest in the Austrian Limestone Alps after 8 and 14 years of soil warming, respectively. Fine root biomass (FRB) and fine root production were 17% and 128% higher in the warmed plots, respectively, after 14 years. The increase in FRB (13%) was not significant after 8 years of treatment, whereas specific root length, specific root area, and root tip density were significantly higher in warmed plots at both sampling occasions. Soil warming did not affect EcM exploration types and diversity, but changed their community composition, with an increase in the relative abundance of Cenoccocum at 0–10 cm soil depth, a drought‐stress‐tolerant genus, and an increase in short‐ and long‐distance exploration types like Sebacina and Boletus at 10–20 cm soil depth. Warming increased the root‐associated bacterial diversity but did not affect their community composition. Soil warming did not affect nutrient concentrations of fine roots, though we found indications of limited soil phosphorus (P) and potassium (K) availability. Our findings suggest that, in the studied ecosystem, global warming could persistently increase soil carbon inputs due to accelerated fine root growth and turnover, and could simultaneously alter fine root morphology and EcM fungal community composition toward improved nutrient foraging.
The consequences of land use intensification and climate warming on productivity, fates of fertilizer nitrogen (N) and the overall soil N balance of montane grasslands remain poorly understood. Here, we report findings of a 15N slurry-tracing experiment on large grassland plant–soil lysimeters exposed to different management intensities (extensive vs. intensive) and climates (control; translocation: +2 °C, reduced precipitation). Surface-applied cattle slurry was enriched with both 15NH4+ and 15N-urea in order to trace its fate in the plant–soil system. Recovery of 15N tracer in plants was low (7–17%), while it was considerably higher in the soil N pool (32–42%), indicating N stabilization in soil organic nitrogen (SON). Total 15N recovery was only 49% ± 7% indicating substantial fertilizer N losses to the environment. With harvest N exports exceeding N fertilization rates, the N balance was negative for all climate and management treatments. Intensive management had an increased deficit relative to extensive management. In contrast, simulated climate change had no significant effects on the grassland N balance. These results suggest a risk of soil N mining in montane grasslands under land use intensification based on broadcast liquid slurry application.
Phosphorus (P) is an essential and often limiting element that could play a crucial role in terrestrial ecosystem responses to climate warming. However, it has yet remained unclear how different P cycling processes are affected by warming. Here we investigate the response of soil P pools and P cycling processes in a mountain forest after 14 years of soil warming (+4 °C). Long-term warming decreased soil total P pools, likely due to higher outputs of P from soils by increasing net plant P uptake and downward transportation of colloidal and particulate P. Warming increased the sorption strength to more recalcitrant soil P fractions (absorbed to iron oxyhydroxides and clays), thereby further reducing bioavailable P in soil solution. As a response, soil microbes enhanced the production of acid phosphatase, though this was not sufficient to avoid decreases of soil bioavailable P and microbial biomass P (and biotic phosphate immobilization). This study therefore highlights how long-term soil warming triggers changes in biotic and abiotic soil P pools and processes, which can potentially aggravate the P constraints of the trees and soil microbes and thereby negatively affect the C sequestration potential of these forests.
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