scholarly journals Dynamic of nitrogen and dissolved organic carbon in an alpine forested catchment: atmospheric deposition and soil solution trends

2019 ◽  
Vol 34 ◽  
pp. 41-66 ◽  
Author(s):  
Raffaella Balestrini ◽  
Carlo Andrea Delconte ◽  
Andrea Buffagni ◽  
Alessio Fumagalli ◽  
Michele Freppaz ◽  
...  

A number of studies have reported decreasing trends of acidifying and N deposition inputs to forest areas throughout Europe and the USA in recent decades. There is a need to assess the responses of the ecosystem to declining atmospheric pollution by monitoring the variations of chemical species in the various compartments of the forest ecosystem on a long temporal scale. In this study, we report on patterns and trends in throughfall deposition concentrations of inorganic N, dissolved organic N (DON) and C (DOC) over a 20-year (1995–2015) period in the LTER site -Val Masino (1190 m a.s.l.), a spruce forest, in the Central Italian Alps. The same chemical species were studied in the litter floor leachates and mineral soil solution, at three different depths (15, 40 and 70 cm), over a 10-year period (2005–2015). Inorganic N concentration was drastically reduced as throughfall and litter floor leachates percolated through the topsoil, where the measured mean values (2 µeq L-1) were much lower than the critical limits established for coniferous stands (14 µeq L-1). The seasonal temperature dependence of throughfall DOC and DON concentration suggests that the microbial community living on the needles was the main source of dissolved organic matter. Most of DOC and DON infiltrating from the litter floor were retained in the mineral soil. The rainfall amount was the only climatic factor exerting a control on DOC and N compounds in throughfall and forest floor leachates over a decadal period. Concentration of SO4 and NO3 declined by 50% and 26% respectively in throughfall deposition. Trends of NO3 and SO4 in forest floor leachates and mineral soil solution mirrored declining depositions. No trends in both DON and DOC concentration and in DOC/DON ratio in soil solutions were observed. These outcomes suggest that the declining NO3 and SO4 atmospheric inputs did not influence the dynamic of DON and DOC in the Val Masino forest. The results of this study are particularly relevant, as they are based on a comprehensive survey of all the main compartments of the forest ecosystem. Moreover, this kind of long-term research has rarely been carried out in the Alpine region.

2003 ◽  
Vol 33 (9) ◽  
pp. 1709-1718 ◽  
Author(s):  
K D Hannam ◽  
C E Prescott

Soluble organic N (SON) is recognized to be a source of N for plants, but the few studies of the effects of clear-cut harvesting on SON levels have reported inconsistent results. SON and soluble inorganic N (SIN) contents were measured in 1 mol/L KCl extracts of soil from forests and clearcuts in coastal cedar–hemlock forests near Port McNeill, B.C., and in high-elevation spruce–fir forests near Sicamous, B.C. To characterize the seedling root environment, sampling was confined to the top 20 cm of soil (consisting of forest floor at Port McNeill and forest floor plus mineral soil at Sicamous). Amino acid N and microbial N were determined on subsets of the samples. At both sites, SON content tended to be lower in clearcuts than in forests. Lower SON contents in clearcuts were caused by the removal of F-layer forest floor at Port McNeill and by reduced SON concentrations in the forest floor at Sicamous. Correlation analyses indicated close relationships between moisture content, SIN, SON, and microbial N. Changes in SON, SIN, and microbial N concentrations during buried bag incubations could not be explained simply by exchange among these three N pools. Free amino acid N accounted for 1–1.5% of the total SON content.


2001 ◽  
Vol 1 ◽  
pp. 457-466 ◽  
Author(s):  
E. Ring ◽  
L. Hogbom ◽  
H.A. Nohrstedt

Biofuels, such as brash from forest fellings, have been proposed as an alternative energy source. Brash removal may affect the sustainability of forest production, e.g., through a change in the availability of cations and N in the soil. We report initial effects of brash removal on inorganic N content in humus and mineral soil, soil-solution chemistry, and field-layer biomass after clear felling an N-fertilisation experiment in central Sweden. The experiment comprised six different fertiliser levels, ranging from 0 to 600 kg N ha�1. Urea was given every 5th year during 1967 to 1982 to replicated plots, giving total doses of 0 to 2400 kg N ha�1. Clear felling took place in 1995, 13 years after the last fertilisation. The removal of brash decreased the NO3� content in the humus layer after clear felling. A decrease in the NO3� concentration of the soil solution was indicated during most of the study period as well. No effect of the previous N fertilisation was found in the humus layer, but in the mineral soil there was an increase in NO3� content for the highest N dose after clear felling (p = 0.06). The soil-solution chemistry and the field-layer biomass showed an irregular pattern with no consistent effects of brash removal or previous fertilisation.


1995 ◽  
Vol 25 (5) ◽  
pp. 833-837 ◽  
Author(s):  
CM. Preston ◽  
D.J. Mead

To follow the movement and transformations of litter-fall N in a forest ecosystem, Douglas-fir (Pseudotsugamenziesii (Mirb.) Franco) foliage labelled with 15N was mixed into the forest floor and left to decompose in steel cylinders of 15 cm diameter X 60 cm length. There were four treatments: 15N-labelled foliage only, foliage plus 200 kg N•ha−1 as urea or NH4NO3, and unamended control. The addition of fertilizer N had no significant effects on 15N recovery or distribution in the soil profile. The overall recovery of 15N to 60 cm depth was 53.7%, 24.9%, and 19.9% after 1, 3, and 7.5 years, respectively. After the first year almost all of the recovered 15N was in the L layer. At 3 years, a higher proportion was found in the FH layer, and by 7.5 years, approximately one-third of the 15N was found in mineral soil horizons. There was very little recovery of 15N in inorganic form (1% or less) after 1 year; in subsequent years inorganic N was found at background levels. Recoveries in soil after 1 and 3 years were similar to those reported for 15N added as inorganic fertilizer in the absence of plant uptake. However, very low losses in the next sampling period (3 to 7.5 years) indicated stabilization of 15N in increasingly recalcitrant forms.


2004 ◽  
Vol 34 (9) ◽  
pp. 1802-1818 ◽  
Author(s):  
Dean F Meason ◽  
Daniel Markewitz ◽  
Rodney E Will

Forest floor organic matter in managed pine forests can accumulate large quantities of N during early stand development. The conversion of the forest floor from a net accumulator to a net source of N as stands age, however, is not well quantified, nor is the effect of management activities on this conversion process. Nitrogen flux from the forest floor of different-aged Pinus taeda L. stands (8, 12, and 14 years old) was measured to understand the impact of annual fertilization (~70 kg N·ha–1·year–1) and complete interspecific competition control on forest floor N cycling. Throughfall and forest floor leachate solutions were collected for 1 year and N mineralization assays conducted. Volume-weighted mean concentrations were used in conjunction with hydrologic fluxes to estimate the net nitrate (NO3–-N), ammonium (NH4+-N), and dissolved organic N flux from the forest floor. Complete competition control had no effect on the inorganic N flux. Changes in inorganic or organic N flux also were not discernable with stand age. Fertilization treatments, excluding fertilizer pulses, significantly increased the forest floor release of N in the fertilized stands compared with the nonfertilized stands (p < 0.05). Overall fluxes of NO3–-N and NH4+-N from the forest floor were, respectively, 2.8 and 6.2 kg N·ha–1·year–1 for fertilized stands and –1.1 and 0.9 kg N·ha–1·year–1 for nonfertilized stands. Unlike inorganic N, organic N was retained in fertilized stands as a result of large organic throughfall inputs. Nitrogen cycling through the forest floor was ~4 kg·ha–1·year–1 greater in fertilized stands. This increased N release may account for as much as 6% of average annual pine demand and thus may well enhance productivity in future years.


2005 ◽  
Vol 35 (2) ◽  
pp. 244-253 ◽  
Author(s):  
T J Fahey ◽  
G L Tierney ◽  
R D Fitzhugh ◽  
G F Wilson ◽  
T G Siccama

Soil C fluxes were measured in a northern hardwood forest ecosystem at the Hubbard Brook Experimental Forest to provide insights into the C balance of soils at this long-term study site. Soil CO2 emission (FCO2) was estimated using a univariate exponential model as a function of soil temperature based on 23 measurement dates over 5 years. Annual FCO2 for the undisturbed northern hardwood forest was estimated at 660 ± 54 g C·m–2·year–1. Low soil moisture significantly reduced FCO2 on three of the measurement dates. The proportion of FCO2 derived from the forest floor horizons was estimated empirically to be about 58%. We estimated that respiration of root tissues contributed about 40% of FCO2, with a higher proportion for mineral soil (46%) than for forest floor (35%). Soil C-balance calculations, based upon evidence that major soil C pools are near steady state at this site, indicated a large C flux associated with root exudation plus allocation to mycorrhizal fungi (80 g C·m–2·year–1, or 17% of total root C allocation); however, uncertainty in this estimate is high owing especially to high error bounds for root respiration flux. The estimated proportion of FCO2 associated with autotrophic activity (52%) was comparable with that reported elsewhere (56%).


2009 ◽  
Vol 6 (12) ◽  
pp. 2743-2758 ◽  
Author(s):  
S. Sleutel ◽  
J. Vandenbruwane ◽  
A. De Schrijver ◽  
K. Wuyts ◽  
B. Moeskops ◽  
...  

Abstract. Numerous recent studies have indicated that dissolved organic carbon (DOC) and nitrogen (DON) play an important role in C and N cycling in natural ecosystems, and have shown that N deposition alters the concentrations and fluxes of dissolved organic substances and may increase leaching losses from forests. Our study was set up to accurately quantify concentrations and flux patterns of DOC, DON and dissolved inorganic nitrogen (DIN) in deciduous and coniferous forest in Flanders, Belgium, under historical high nitrogen deposition. We measured DOC, DON and DIN concentrations at two weekly intervals in a silver birch (SB) stand, a corsican pine (CP) stand and a pine stand with higher N deposition (CPN), and used the SWAP model (calibrated with PEST) for generating accurate water and matter fluxes. The input with precipitation was an important source of DON, but not for DOC. Release of DOC from the forest floor was minimally affected by forest type, but higher N deposition (CPN stand) caused an 82% increase of DOC release from the forest floor. Adsorption to mineral soil material rich in iron and/or aluminum oxyhydroxides was suggested to be the most important process removing DOC from the soil solution, responsible for substantial retention (67–84%) of DOC entering the mineral soil profile with forest floor leachate. Generally, DON was less reactive (i.e. less removal from the soil solution) than DOC, resulting in decreasing DOC/DON ratios with soil depth. We found increased DOC retention in the mineral soil as a result of higher N deposition (84 kg ha−1 yr−1 additional DOC retention in CPN compared to CP). Overall DON leaching losses were 2.2, 3.3 and 5.0 kg N yr−1 for SB, CP and CPN, respectively, contributing between 9–28% to total dissolved N (TDN) leaching. The relative contribution to TDN leaching from DON loss from SB and CP was mainly determined by (large) differences in DIN leaching. The large TDN leaching losses are alarming, especially in the CPN stand that was N saturated.


2019 ◽  
Author(s):  
Daniel A. Petrash ◽  
Frantisek Buzek ◽  
Martin Novak ◽  
Bohuslava Cejkova ◽  
Pavel Kram ◽  
...  

Abstract. In order to interpret spatial patterns of soil nutrient partitioning and compare these with runoff in a temperate forest with a history of acidification-related spruce die-back, the chemistry of mineral soil solutions were collected by suction lysimeters and evaluated relative to concurrent loads of anions and cations in precipitation. Lysimeters nest were installed in the 33-ha U dvou loucek (UDL) mountain catchment at different topographic positions (hilltops, slopes and valley). Following equilibration, monthly soil solution samples were collected over a 2-year period. In the vicinity of each lysimeter nest, soil pits were excavated for constraining soil chemistry. Soil solutions were analyzed for SO42−, NO3−, NH4+, Na+, K+, Ca2+, Mg2+, and total dissolved Al concentrations and organic matter (DOC), and pH. For a P release estimation, ammonium oxalate extraction of soil samples was performed. Comparison of soil water data with other previously acidified monitored European sites indicated that environmentally relevant chemical species at UDL had concentrations similar to median concentrations observed in sites with similar bedrock lithology and vegetation cover. Cation exchange capacity (CEC ≤ 58 meq kg−1) and base saturation (BS ≤ 13 %), however, were significantly lower at UDL, documenting incomplete recovery from acidification. Spatial trends and seasonality in soil water chemistry support belowground inputs from mineral-stabilized legacy pollutants. Overall, the soil-solution data suggest the system is out of balance chemically, relative to the present loads of anions and cations in precipitation. Higher concentrations of SO42−, NO3−, and base cations in runoff than in soil solutions are explained by lateral surficial leaching of pollutants and nutrients from shallow soil horizons. Nearly 30 years after peak acidification, UDL exhibited similar soil solution concentrations of SO42, Ca2+ and Mg2+ as median values at the Pan-European International Co-operative Program (ICP) Forest sites, yet NO3− concentrations were an order of magnitude higher.


2009 ◽  
Vol 6 (4) ◽  
pp. 7133-7173 ◽  
Author(s):  
S. Sleutel ◽  
J. Vandenbruwane ◽  
A. De Schrijver ◽  
K. Wuyts ◽  
B. Moeskops ◽  
...  

Abstract. Numerous recent studies have indicated that dissolved organic carbon (DOC) and nitrogen (DON) play an important role in C and N cycling in natural ecosystems, and have shown that N deposition alters the concentrations and fluxes of dissolved organic substances and may increase leaching losses from forests. Our study was set up to accurately quantify concentrations and flux patterns of DOC, DON and dissolved inorganic nitrogen (DIN) in deciduous and coniferous forest in Flanders under historical high nitrogen deposition. We measured DOC, DON and DIN concentrations at two weekly intervals in a silver birch (SB) stand, a corsican pine (CP) stand and a pine stand with higher N deposition (CPN), and used the SWAP model (calibrated with PEST) for generating accurate water and matter fluxes. The input with precipitation was an important source of DON, but not for DOC. Release of DOC from the forest floor was minimally affected by forest type, but higher N deposition (CPN stand) caused an 82% increase of DOC release from the forest floor. Adsorption to mineral soil material rich in iron and/or aluminum oxyhydroxides was suggested to be the most important process removing DOC from the soil solution, responsible for substantial retention (67–84%) of DOC entering the mineral soil profile with forest floor leachate. Generally, DON was less reactive (i.e. less removal from the soil solution) than DOC, resulting in decreasing DOC/DON ratios with soil depth. We found increased DOC retention in the mineral soil as a result of higher N deposition (84 kg N ha−1 yr−1 additional DOC retention in CPN compared to CP). Overall DON leaching losses were 2.2, 3.3 and 5.0 kg N ha−1 yr−1 for SB, CP and CPN, respectively, contributing between 9–28% to total dissolved N (TDN) leaching. DON loss from SB and CP was not much higher than from unpolluted forests, and its relative contribution to TDN leaching was mainly determined by (large) differences in DIN leaching. The large TDN leaching losses are alarming, especially in the CPN stand that was N saturated.


2021 ◽  
Vol 18 (3) ◽  
pp. 1009-1027 ◽  
Author(s):  
Michael Rinderer ◽  
Jaane Krüger ◽  
Friederike Lang ◽  
Heike Puhlmann ◽  
Markus Weiler

Abstract. The phosphorus (P) concentration of soil solution is of key importance for plant nutrition. During large rainfall events, the P concentration is altered by lateral and vertical subsurface storm flow (SSF) that facilitates P mobilization, redistribution within the soil profile and potential P export from the ecosystem. These processes are not well studied under field conditions. Important factors of the replenishment of P concentrations in soil solutions are the rate of P replenishment (by biotic and abiotic processes) and the P buffering capacity of soils. Lab experiments have shown that replenishment times can vary between minutes and months. The question remains of how P concentrations in lateral and vertical SSF vary under natural field conditions. We present results of large-scale sprinkling experiments simulating 150 mm throughfall at 200 m2 plots on hillslopes at three beech forests in Germany. We aimed at quantifying lateral and vertical SSF and associated P concentrations on the forest floor, in the mineral soil and in the saprolite during sprinkling experiments in spring and summer. The sites differed mainly in terms of soil depth, skeleton content and soil P stock (between 189 and 624 g/m2 in the top 1 m soil depth). Vertical SSF in the mineral soil and in the saprolite was at least 2 orders of magnitude larger than lateral SSF at the same depth. Vertical and lateral SSF consisted mainly of pre-event water that was replaced by sprinkling water. Higher P concentrations in SSF in the first 1 to 2 h after the onset of SSF indicated nutrient flushing, but P concentrations in the mineral soil and saprolite were nearly constant thereafter for most of the experiment despite a strong increase in SSF. This suggests that P in the soil solution at all three sites was replenished fast by mineral or organic sources. If chemostatic transport conditions would dominate in SSF, annual P losses at the lateral and vertical boundary of a forest plot could be approximated by knowing the average P concentration and the water fluxes in forest soils. A rough estimation of the annual P loss based on this simplified assumption for one of our sites with longer SSF data resulted in an annual P loss of 3.16 mg/m2/a. This P loss is similar to estimates from a previous study at the same site using bi-weekly groundwater samples. Our approximated annual P loss in SSF was in a similar order of magnitude as P input by dry and wet deposition and by mineral weathering. Despite the fact that P losses from the ecosystem seem to be small, the translocation of P from the forest floor to the mineral soil might be of high relevance at sites with low P stocks where the forest floor is the dominant source for the P nutrition of trees.


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