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In recent years, important processes controlling ecosystem carbon dynamics have been connected to fine-root exudation of soluble carbon compounds. Root exudation patterns may change depending on plant interactions and plant susceptibility to and recovery from drought. Recent investigations suggest that root exudation tends to increase with stress events, but quantification of the amount of carbon released from roots across soil depths with differing water availability and species interactions are missing.We tested if root exudation rates were negatively correlated with soil water content across soil depths during and after drought. We further tested if species in mixture, often considered to be less stressed under drought, exuded less carbon than species in monospecific environments. Exudates were sampled in a mature Fagus sylvatica L. and Picea abies (L.) Karst. forest at the end of a five-year throughfall exclusion period and again one year after the drought ended. We quantified root exudates and their variation with soil depth for both tree species in monospecific and mixed species zones.Carbon exudation significantly increased in fine roots exposed to dry soils (

Forest soils are crucial for many ecosystem services that rely on soil organic matter (SOM) stability. Carbon allocated to roots and released as exudates to the rhizosphere plays a key role in SOM stabilization. Under periodic drought, elevated root exudation and SOM accumulation have been reported. Yet, whether root exudates control SOM formation and stability in mature forests once the drought ends is largely unknown. We examined whether root exudates from P. abies and F. sylvatica trees relate to SOM formation and stability in soil depth profiles one year following five years of experimental drought (Kroof experiment, Germany). We collected root exudates throughout the rooting zone and combined the data with thermogravimetric analysis of SOM in the rhizosphere and non-rooted soil. We found that the rhizosphere of both species was characterized by stable SOM fractions that did not decrease post-drought, suggesting potential protection of SOM due to rhizodeposition and root exudates. In contrast, stable SOM fractions decreased relative to controls in non-rooted topsoil below P. abies, indicating a loss of stabilized SOM from drought-affected and re-wetted soil. Our measurements provide valuable insights into post-drought SOM formation and mechanisms of SOM stabilization in forest ecosystems under climate change.

As climate change progresses, the frequency and duration of drought stress events are increasing. While the mechanisms of drought acclimation of trees has received considerable attention in recent years, the recovery processes remain critically understudied. We used a unique throughfall exclusion experiment in a mature temperate mixed forest consisting of the more isohydric Norway spruce and more anisohydric European beech, to study the recovery and resilience after drought release. We hypothesized that pre-dawn water potential (ΨPD) of both species will increase within 1 day after watering, while the recovery of stomatal conductance (gs) and the reversal of osmoregulation will be significantly delayed in the more isohydric spruce. Furthermore, we hypothesized that the xylem sap flow density (udaily) will not fully recover within the growing season due to the strong drought impact. After 5 years of summer drought, trees showed significantly reduced ΨPD, udaily and increased osmoregulation in leaves, but only isohydric spruce displayed increased leaf abscisic acid concentrations. In line with our hypothesis, ΨPD and gs recovered within 1 day in beech. Conversely, isohydric spruce showed delayed increases in ΨPD and gs. The delay in recovery of spruce was partially related to the replenishment of the stem water reservoir, as indicated by the missing response of udaily at the crown base compared with DBH level upon watering. However, udaily fully recovered only in the next growing season for beech and was still reduced in spruce. Nevertheless, in both species, osmotic acclimations of leaves were reversed within several weeks. While both species displayed full resilience to drought stress in water-related physiology, the recovery time was in several cases, e.g., udaily, ΨPD and gs, shorter for beech than for spruce. With future increases in the frequency of drought events under ongoing climate change, tree species that recover more quickly will be favored.

Acclimation processes in a changing climate require the ability to tolerate and survive abiotic stress events (e.g. drought), challenging especially immobile and long-living species and ecosystems, such as forests. The drought years 2018/2019 in Central Europe have laid bare the vulnerability of temperate forest ecosystems to drought and heat. The recovery phase after the stress event represents a crucial phase, especially after intense and repeated drought periods, and might be different for anisohydric and isohydric species.The second phase of the Kranzberg Forest Roof (KROOF) experiment in southeast Germany focused on the watering of mature more anisohydric European beech (Fagus sylvatica L.) and more isohydric Norway spruce (Picea abies (L.) H. Karst.) after five years of repeated experimental summer drought. Both treatments, the former throughfall-exclusion (TE, recovering trees) and control (CO) plots were labeled with 2H enriched water by controlled watering, to end the experimental drought. Pre-dawn leaf water potential, stomatal conductance, xylem sap flow density (at breast height and crown base) and leaf osmoregulation were recorded for two growing seasons after drought release and the resilience and recovery times were calculated. All measured parameters were strongly reduced by on average 30% in both species due to the drought treatment. While the distribution of the labeled water upon irrigation across the soil profile occurred within a few days in both treatments, the water uptake and distribution within the trees was delayed by several days in recovering trees compared to control trees and in recovering spruce compared to recovering beech. Additionally, upon drought release recovering beech reached full resilience (i.e. same level as control trees) earlier than recovering spruce in water potential, stomatal conductance and xylem sap flow density and even showed signs of overcompensation by surpassing the control trees. No differences were found between the two species in the recovery of leaf osmoregulation.The “opposing” drought mitigation strategies seem to be responsible for the differences detected between more anisohydric beech and spruce during the recovery period. For example, the lack of recovery of xylem sap flow density at crown base in TE spruce indicates a re-filling of the stem water reservoirs upon watering. Additionally, we found fast responding parameters as water potential (hours to days) and stomatal conductance (days to weeks) compared to slow responding parameters such as osmoregulation (weeks to months) and full hydraulic recovery, i.e. xylem sap flow density, may even take years. Rapid physiological recovery after drought events, which are expected to increase in frequency and intensity with ongoing climate change, will be beneficial for overall recovery and might put faster-reacting trees in favor over slower responding species.

Drought is a severe natural risk that increases drying-rewetting frequencies of soils. Yet, it remains largely unknown how forest ecosystems respond to dry-wet cycles, hampering our ability to evaluate the overall sink and source functionality for this large carbon pool. Recent investigations suggest that the release of soluble carbon via root exudation increases under drought, influencing soil carbon stabilization and mineralization. However, an integration of root exudation into the carbon allocation dynamics of drought stressed trees is missing. We hypothesized that roots in dry soil layers have a higher exudation rate than roots in more moist layers across different soil depths. Further, we tested if higher exudation rates under drought are attenuated by reduced root abundance in dry soils and if the fraction of root exudation from total carbon allocation increases with decreasing photosynthesis rates under drought. At the KROOF experimental site in southern Germany, where mature beech (Fagus sylvatica L.) and spruce (Picea abies (L.) Karst.) trees were exposed to artificial drought stress for five consecutive growing seasons, we show that at the root level root exudation rate increases in drier soils. Especially roots in the upper soil profile and roots of spruce trees increased root exudation under drought. When scaled to whole tree level, we did not find differences in total exudation between drought stressed and control trees, indicating sustained root exudation at the tree level under drought. As photosynthesis rates and therefore total carbon assimilation was substantially reduced under drought (by 50 % in beech and almost 70 % in spruce), the fraction of root exudation from total assimilation slightly increased for drought stressed trees. Our results demonstrate that stimulation of root exudation rates with drought exists in natural temperate forest ecosystems but might be mitigated by reduced fine root abundance under drought. Nevertheless, increased exudation per root surface area will have localized impacts on rhizosphere microbial composition and activity especially in the topsoil exposed to more extreme dry-wet cycles. Finally, also the exudate composition can help to determine how priming of soil organic matter relates to belowground carbon allocation dynamics and to disclose processes of complementary species interaction and should be emphasised in future studies.

This contribution presents the result of a free-air 13C labeling experiment on mature Norway spruce (P. abies [L.] KARST.) upon watering after five years of recurrent summer drought in southern Germany, focusing on whole tree allocation processes. Mature spruce trees had been exposed to recurrent summer drought from 2014 to 2018 through complete exclusion of precipitation throughfall from spring to late fall (i.e., March to November). In early summer 2019, the drought stressed spruce trees were watered to investigate their recovery processes. In parallel with the watering, we conducted a whole-tree 13C labeling in canopies and traced the signal in various C sinks, i.e. stem phloem and CO2 efflux, tree rings at different heights, coarse roots, fine root tips, mycorrhiza, root exudates, and soil CO2 efflux.We hypothesize that drought stressed spruce preferentially allocates newly assimilated C to belowground sinks upon drought release. Conversely to our expectations, allocation to belowground C sinks was not stimulated in drought stressed compared to control spruce. Likewise, the relative amount of recently fixed C allocated to aboveground sinks did not differ between treatments. Our findings suggest that the belowground C sinks are not of higher priority for the allocation of newly assimilated C upon watering after long-term drought. The observed allocation pattern is discussed taking total above- and belowground biomass as well as C source/sink relations into account.

Tracers provide a way to determine, follow and quantify biochemical cycles and energy fluxes within the soil-plant-atmosphere continuum (SPAC). Thereby, different tracers, such as dyes, carbonyl sulfite or stable isotopes are employed. One major disadvantage of many tracers is, that very often, plants have to be destructively harvested to analyze the tracer concentration, making it difficult to measure continuous fluxes. Additionally, for stable isotope studies, fractionation or exchange effects can make interpretation and quantification of biogeochemical fluxes difficult. Novel tracers that are already frequently used in animal systems, are fluorescent C-dots. These nanoparticles (5-50 nm diameter) provide a non-destructive imaging option using “in vivo imaging systems” (IVIS). We examined a first approach to apply and measure C-dots as possible tracers in tree saplings of three species (Picea glauca, Pinus strobus, Tsuga canadensis). Roots were excavated from soils and exposed to 20 µmol/l liquid silica-based nanoparticles (diameter of 5.1 nm) labeled with a near-infrared fluorophore, cyanine 5.5 (excitation maximum 646 nm, emission maximum 662 nm). Subsequent continuous IVIS imaging showed real-time uptake and transport of the C-dots by the trees. Respective fluorescence intensity revealed the concentration of C-dots in each of the tissues at measured time steps. Subsequent cross-sectioning of roots, stems and leaves elucidated the internal transport pathway of the C-dots inside the saplings’ tissues. Finally, measurements of stomatal conductance, photosynthesis, transpiration rate, stem hydraulic conductivity and pre-dawn leaf water potentials in comparison to control saplings revealed no phytotoxic effect by the C-dots on plant functioning. In conclusion, C-dots provide a non-toxic new technique for measuring biochemical cycles within the SPAC. Future applications include high resolution tracing of water flow cycles and turnover times within the SPAC, compound specific analyses of root exudation or determining mechanisms of pest influences on plant metabolism.

Forest cover exerts a significant control on the partitioning of precipitation between evapotranspiration and surface runoff. Thus, understanding how plants take up and transpire water in forested catchments is essential to predict flooding potential and hydrologic cycling. A growing literature underscores the importance of integrating whole-plant hydraulics, including such processes as the spatial variability of root distribution and the temporally dynamic nature of root water uptake by depth in understanding the relationship between changes in vegetation and hydrology. The analysis of stable isotopes of water (18O and 2H) sourced from soils and plant tissue has enabled the estimation of tree root water uptake depths and water use strategies. Despite the general acceptance of stable water isotopic data to estimate plant hydraulic dynamics, this methodology imposes assumptions that may produce spurious results. For example, end member mixing analysis neglects time-delays during tree-water storage. Also, it is likely that hydraulic redistribution processes of plants, which transport water across soil depths and both into and out of plant tissue, modify δ18O and δ2H; the isotopic signature of a collected sample may thus reflect a history of transport and exposure to fractionating processes not accounted for in analysis. We tested the feasibility of C-dots, core-shell silica polyethylene-glycol coated fluorescent nano-particles (5.1 nm diameter) in 20 µmol/l solution with H2O labeled with a near-infrared fluorophore, cyanine 5.5 (excitation maximum of 646 nm, emission maximum of 662 nm), as an alternative to stable water isotopes in the investigation of plant hydraulics. We examined the absorption and transport of C-dots through soil, as well as roots and aerial structures of Eastern hemlock (Tsuga canadensis), Eastern white pine (Pinus strobus), and white spruce (Picea glauca) saplings (n = 12 each) via an IVIS-200 luminescence in-situ imaging system. We compared the fluid mechanics, residence times and mixing schemes of C-dots with 2H-labeled water during transport within these plant species to establish the nanoparticles as a viable alternative through a split-root hydraulic redistribution experiment under moderate and severe drought conditions. We present a residence-time distribution to elucidate the mixing scheme of C-dot solution and calibration curves to aid future studies. This research is the premier assessment of this nanoparticle as an alternative tracer to stable water isotopes, and as such may yield insights for broader applications.

Hydraulic redistribution (HR) of soil water through plant roots is a crucial phenomenon improving the water balance of plants and ecosystems. It is mostly described under severe drought, and not yet studied under moderate drought. We tested the potential of HR under moderate drought, hypothesizing that (H1) tree species redistribute soil water in their roots even under moderate drought and that (H2) neighboring plants are supported with water provided by redistributing plants. Trees were planted in split-root systems with one individual (i.e., split-root plant, SRP) having its roots divided between two pots with one additional tree each. Species were 2- to 4-year-old English oak (Quercus robur L.), European beech (Fagus sylvatica L.) and Norway spruce (Picea abies (L.) Karst). A gradient in soil water potential (ψsoil) was established between the two pots (-0.55 ± 0.02 MPa and -0.29 ± 0.03 MPa), and HR was observed by labeling with deuterium-enriched water. Irrespective of species identity, 93% of the SRPs redistributed deuterium enriched water from the moist to the drier side, supporting H1. Eighty-eight percent of the plants in the drier pots were deuterium enriched in their roots, with 61 ± 6% of the root water originating from SRP roots. Differences in HR among species were related to their root anatomy with diffuse-porous xylem structure in both beech and-opposing the stem structure-oak roots. In spruce, we found exclusively tracheids. We conclude that water can be redistributed within roots of different tree species along a moderate ψsoil gradient, accentuating HR as an important water source for drought-stressed plants, with potential implications for ecohydrological and plant physiological sciences. It remains to be shown to what extent HR occurs under field conditions in Central Europe.

Hydraulic redistribution (HR) of soil water through plant roots is widely described; however its extent, especially in temperate trees, remains unclear. Here, we quantified HR of five temperate tree species. We hypothesized that both, HR within a plant and into the soil increase with higher water‐potential gradients, larger root conduit diameters and root‐xylem hydraulic conductivities as HR driving factors. Saplings of conifer (Picea abies, Pseudotsuga menziesii), diffuse‐porous (Acer pseudoplatanus) and ring‐porous species (Castanea sativa, Quercus robur) were planted in split‐root systems, where one plant had its roots split between two pots with different water‐potential gradients (0.23–4.20 MPa). We quantified HR via deuterium labelling. Species redistributed 0.39 ± 0.14 ml of water overnight (0.08 ± 0.01 ml/g root mass). Higher pre‐dawn water‐potential gradients, hydraulic conductivities and larger conduits significantly increased HR quantity. Hydraulic conductivity was the most important driving factor on HR amounts, within the plants (0.03 ± 0.01 ml/g) and into the soil (0.06 ± 0.01 ml/g). Additional factors as soil‐root contact should be considered, especially when calculating water transfer into the soil. Nevertheless, trees maintaining high‐xylem hydraulic conductivity showed higher HR amounts, potentially making them valuable ‘silvicultural tools’ to improve plant water status. A free Plain Language Summary can be found within the Supporting Information of this article.

Hydraulic redistribution (HR) can buffer drought events of tree individuals, however, its relevance for neighbouring trees remains unclear. Here, we quantified HR to neighbouring trees in single- and mixed-species combinations. We hypothesized that uptake of HR water positively correlates with root length, number of root tips and root xylem hydraulic conductivity and that neighbours in single-species combinations receive more HR water than in phylogenetic distant mixed-species combinations. In a split-root experiment, a sapling with its roots split between two pots redistributed deuterium labelled water from a moist to a dry pot with an additional tree each. We quantified HR water received by the sapling in the dry pot for six temperate tree species. After 7 days, one quarter of the water in roots (2.1 ± 0.4 ml), stems (0.8 ± 0.2 ml) and transpiration (1.0 ± 0.3 ml) of the drought stressed sapling originated from HR. The amount of HR water transpired by the receiving plant stayed constant throughout the experiment. While the uptake of HR water increased with root length, species identity did not affect HR as saplings of Picea abies ((L.) Karst) and Fagus sylvatica (L.) in single- and mixed-species combinations received the same amount of HR water.