Carbon and nitrogen transformations in New Zealand plantation forest soils from sites with different N status

1998 ◽  
Vol 28 (7) ◽  
pp. 967-976 ◽  
Author(s):  
Neal A Scott ◽  
Roger L Parfitt ◽  
Des J Ross ◽  
Gareth J Salt

Interactions between soil nutrient cycling processes are likely to influence N losses following disturbance in forest ecosystems. During a 340-day laboratory incubation, we examined C and N transformations in three sandy soils of different N status from Pinus radiata D. Don plantations before clear-cutting. The soils were a high N status Andisol (losing -N in streamwater) and a fertilized and unfertilized Entisol. In contrast to other forest ecosystems, -N accumulated readily in all mineral soils and in the Andisol forest floor but did not accumulate until day 63 and 210 in the fertilized and unfertilized Entisol forest floor, respectively. However, gross nitrification occurred from day 42 in both Entisol treatments. Net nitrification in the Entisol forest floor began when substrate C/N ratio declined to about 40, possibly because of decreased C availability and decreased competition for both -N and -N in conjunction with a lower microbial C/N ratio. Carbon and gross N mineralization rates (per unit of C or N, respectively) correlated positively (r2 = 0.93) in mineral soil but correlated negatively in the forest floor, probably because of major differences in C and N quality and potential differences in microbial community structure. The mean residence time of N in mineral-N pools was higher for soils from the N-rich site, in part because of lower microbial N demand. These results suggest that sudden removal of C inputs (such as at harvest) may cause greater disruption of internal soil N cycles on nutrient poor sites, increasing the proportional losses of N as compared to nutrient-rich sites.

2008 ◽  
Vol 54 (No. 8) ◽  
pp. 377-387
Author(s):  
P. Sah S ◽  
R. Brumme ◽  
N. Lamersdorf

We analysed stable isotopes of N in a spruce forest under ambient rainfall (no further manipulation of the atmospheric input) and clean rain application (10 years of reduced inorganic N- and acid-constituent input). The objectives of the study were to assess whether or not the natural <sup>15</sup>N abundance would function as an indicator for the N-status of our forest ecosystems. For this purpose, natural <sup>15</sup>N abundance values were measured in needles, litter fall, roots, soil, bulk precipitation, throughfall and soil water of both plots. In the bulk precipitation and throughfall the &delta;<sup>15</sup>N values of NO<sub>3</sub>-N were in the range reported by other studies (–16 to + 23‰). In both plots, the throughfall was greatly depleted of <sup>15</sup>N compared to the bulk precipitation and this was attributed to nitrification in the canopy leaves, leading to &delta;<sup>15</sup>N-depleted nitrate production in the leaves that leaches down the soil surface. Nitrate in seepage water showed a general increase in &delta;<sup>15</sup>N values when it passes through the upper mineral soil (10 cm soil depth) and infiltrates into deeper mineral soil horizons (100 cm soil depth), similar to the &delta;<sup>15</sup>N enrichment of total nitrogen in the mineral soil. We observed <sup>15</sup>N depletion in both green needles and litter fall at the clean rain plot, compared to the N-saturated control plot. We assumed it to be due to increased mycorrhizal N-uptake under N limited, i.e. clean rain conditions which are indicated by relatively lower N concentrations of green needles. With respect to the vertical gradient of the <sup>15</sup>N abundance in the forest floor, both plots differ from each other, showing an untypical peak of &delta;<sup>15</sup>N depletion in the humus layer, which is more pronounced at the control plot. In contrast to the mineral soil where mineralisation is a dominant process for fractionation we attribute the &delta;<sup>15</sup>N pattern in the forest floor to additional processes like litter input and immobilisation. We conclude that the &delta;<sup>15</sup>N natural abundance analysis is helpful for interpreting the N-status of forest ecosystems but further research is needed especially with respect to the soil-root interface.


2019 ◽  
Author(s):  
Jörg Matschullat ◽  
Roberval Monteiro Bezerra de Lima ◽  
Sophie F. von Fromm ◽  
Solveig Pospiech ◽  
Andrea M. Ramos ◽  
...  

Abstract. Given the dimensions of the Amazon basin (7.5 million km2), its internal dynamics, increasing anthropogenic strain on this large biome, and its global role as one of two continental biospheric tipping elements, it appears crucial to have data-based knowledge on carbon and nitrogen concentrations and pools as well as on possible intra-annual dynamics. We quantified carbon (Ct, Corg), nitrogen (N) and sulfur (S) concentrations in litter (ORG) and mineral soil material (TOP 0–20 cm, BOT 30–50 cm) of upland (terra firme) oxisols across Amazonas state and present a first pool calculation. Data are based on triplicate seasonal sampling at 29 sites (forest and post-forest) within the binational project EcoRespira-Amazon (ERA). Repeated sampling increased data accuracy and allows for interpreting intra-annual (seasonal) and climate-change related dynamics. Extreme conditions between the dry season in 2016 and the subsequent wet season (ENSO-related) show differences more clearly. Median CNS in the Amazon basin TOP soils (Ct 1.9, Corg 1.6, N 0.15, S 0.03 wt-% under forest canopy) as well as Corg / N ratios show concentrations similar to European soils (FOREGS, GEMAS). TOP Ct concentrations ranged from 1.02 to 3.29 wt-% (medianForest 2.17 wt-%; medianPost-Forest 1.75 wt-%), N from 0.088 to 0.233 wt-% (medianForest 0.17 wt-%; medianPost-Forest 0.09 wt-%) and S from 0.012 to 0.051 wt.-% (medianForest 0.03 wt.-%; medianPost-Forest 0.02 wt-%). Corg / N ratios ranged from 6 to 14 (median 10). A first pool calculation (hectare-based) illustrates forest versus post-forest changes. The elements are unevenly distributed in the basin with generally higher CNS values in the central part (Amazonas graben) as compared to the southern part of the basin. Deforestation and drought conditions lead to C and N losses – within 50 years after deforestation, C and N losses average 10 to 15 %. Regional climate change with increased drought will likely speed up carbon and nitrogen losses.


Forests ◽  
2020 ◽  
Vol 11 (10) ◽  
pp. 1040
Author(s):  
R. Kasten Dumroese ◽  
Martin F. Jurgensen ◽  
Deborah S. Page-Dumroese

Research Highlights: This experiment compares a range of combinations of harvest, prescribed fire, and wildfire. Leveraging a 30-year-old forest management-driven experiment, we explored the recovery of woody species composition, regeneration of the charismatic forest tree species Larix occidentalis Nutt., and vegetation and soil carbon (C) and nitrogen (N) pools. Background and Objectives: Initiated in 1967, this experiment intended to explore combinations of habitat type phases and prescribed fire severity toward supporting regeneration of L. occidentalis. At onset of the experiment, a wildfire affected a portion of the 60 research plots, allowing for additional study. Our objective was to better understand silvicultural practices to support L. occidentalis regeneration and to better understand the subsequent impacts of silvicultural practices on C and N pools within the vegetation and soil. Materials and Methods: We categorized disturbance severity based on loss of forest floor depth; 11 categories were defined, including controls for the two habitat type phases involved. We collected abundance, biomass, and C and N concentrations for the herbaceous layer, shrubs, and trees using nested quadrats and 6 to 10 experimental units per disturbance category plot. Moreover, we systematically sampled woody residue from transects, and forest floor, soil wood, and mineral soil with a systematic grid of 16 soil cores per disturbance category plot. Results: We found that (1) disturbance severity affected shrub species richness, diversity, and evenness within habitat type phases; (2) L. occidentalis regenerates when fire is part of the disturbance; (3) N-fixing shrub species were more diverse in the hotter, drier plots; (4) recovery levels of C and N pools within the soil had surpassed or were closer to pre-disturbance levels than pools within the vegetation. Conclusions: We confirm that L. occidentalis regeneration and a diverse suite of understory shrub species can be supported by harvest and prescribed fire, particularly in southern and western aspects. We also conclude that these methods can regenerate L. occidentalis in cooler, moister sites, which may be important as this species’ climate niche shifts with climate change.


2012 ◽  
Vol 42 (3) ◽  
pp. 585-592 ◽  
Author(s):  
Sven Wirthner ◽  
Martin Schütz ◽  
Deborah S. Page-Dumroese ◽  
Matt D. Busse ◽  
James W. Kirchner ◽  
...  

Recovering from small fragmented populations, wild boars ( Sus scrofa L.) have considerably increased their numbers and their habitat range in many European countries during the past two decades. Although several studies have focused on the impact of wild boar rooting on selected vegetation properties, little is known about effects on entire forest ecosystems. The main goal of our study was to assess how rooting by boars alters soil and vegetation properties. We measured soil chemical and biological properties (C and N concentrations, N availability, and microbial biomass C) as well as several vegetation characteristics (total plant cover, plant species diversity, and number and height of saplings) on paired rooted and non-rooted plots in six hardwood forests in Switzerland. We found that rooting by wild boars led to significant increases in mineral soil C and N concentrations and microbial biomass C, which could lead to improved growth conditions for plants. However, total plant cover and sapling counts were reduced on rooted plots, possibly due to mechanical disturbance or due to reduced plant available N (measured as supply rate in contrast with the observed increase in total stocks of mineral soil N). In view of these results, simple characterizations of wild boar rooting as beneficial or detrimental to forest ecosystems should be handled with care.


2016 ◽  
Vol 83 (1) ◽  
Author(s):  
Yun-Feng Duan ◽  
Xian-Wang Kong ◽  
Andreas Schramm ◽  
Rodrigo Labouriau ◽  
Jørgen Eriksen ◽  
...  

ABSTRACT Grassland cultivation can mobilize large pools of N in the soil, with the potential for N leaching and N2O emissions. Spraying with the nitrification inhibitor 3,4-dimethylpyrazole phosphate (DMPP) before cultivation was simulated by use of soil columns in which the residue distribution corresponded to plowing or rotovation to study the effects of soil-residue contact on N transformations. DMPP was sprayed on aboveground parts of ryegrass and white clover plants before incorporation. During a 42-day incubation, soil mineral N dynamics, potential ammonia oxidation (PAO), denitrifying enzyme activity (DEA), nitrifier and denitrifier populations, and N2O emissions were investigated. The soil NO3 − pool was enriched with 15N to trace sources of N2O. Ammonium was rapidly released from decomposing residues, and PAO was stimulated in soil near residues. DMPP effectively reduced NH4 + transformation irrespective of residue distribution. Ammonia-oxidizing archaea (AOA) and bacteria (AOB) were both present, but only the AOB amoA transcript abundance correlated with PAO. DMPP inhibited the transcription of AOB amoA genes. Denitrifier genes and transcripts (nirK, nirS, and clades I and II of nosZ) were recovered, and a correlation was found between nirS mRNA and DEA. DMPP showed no adverse effects on the abundance or activity of denitrifiers. The 15N enrichment of N2O showed that denitrification was responsible for 80 to 90% of emissions. With support from a control experiment without NO3 − amendment, it was concluded that DMPP will generally reduce the potential for leaching of residue-derived N, whereas the effect of DMPP on N2O emissions will be significant only when soil NO3 − availability is limiting. IMPORTANCE Residue incorporation following grassland cultivation can lead to mobilization of large pools of N and potentially to significant N losses via leaching and N2O emissions. This study proposed a mitigation strategy of applying 3,4-dimethylpyrazole phosphate (DMPP) prior to grassland cultivation and investigated its efficacy in a laboratory incubation study. DMPP inhibited the growth and activity of ammonia-oxidizing bacteria but had no adverse effects on ammonia-oxidizing archaea and denitrifiers. DMPP can effectively reduce the potential for leaching of NO3 − derived from residue decomposition, while the effect on reducing N2O emissions will be significant only when soil NO3 − availability is limiting. Our findings provide insight into how DMPP affects soil nitrifier and denitrifier populations and have direct implications for improving N use efficiency and reducing environmental impacts during grassland cultivation.


2010 ◽  
Vol 42 (8) ◽  
pp. 1303-1312 ◽  
Author(s):  
Jan Muhr ◽  
Janine Franke ◽  
Werner Borken

1984 ◽  
Vol 14 (6) ◽  
pp. 763-767 ◽  
Author(s):  
C. Anthony Federer

Organic content of the forest floor decreases for several years after clear-cutting, and then slowly recovers. Thickness, bulk density, organic matter, and nitrogen content of forest floors were measured for 13 northern hardwood stands in the White Mountains of New Hampshire. Stands ranged from 1 to about 100 years in age. Forest-floor thickness varied significantly with stand age, but bulk density, organic fraction, and nitrogen fraction were independent of age. Total organic content of the forest floor agreed very well with data from Covington's (W. W. Covington 1981. Ecology, 62: 41–48) study of the same area. Both studies indicated that mature forest floors have about 80 Mg organic matter•ha−1 and 1.9 Mg nitrogen•ha−1. Within 10 or 15 years after cutting, the organic matter content of the floor decreases to 50 Mg•ha−1, and its nitrogen content to 1.1 Mg•ha−1. The question whether the decrease is rapid and the minimum broad and flat, or if the decrease is gradual and the minimum sharp, cannot be answered. The subsequent increase to levels reached in mature forest requires about 50 years. Some of the initial decrease in organic matter and nitrogen content of the forest floor may be caused by organic decomposition and nitrogen leaching, but mechanical and chemical mixing of floor into mineral soil, during and after the harvest operation, may also be important. The difference is vital with respect to maintenance of long-term productivity.


Author(s):  
Daniel J. Dall’Orsoletta ◽  
Luiz P. Rauber ◽  
Djalma E. Schmitt ◽  
Luciano C. Gatiboni ◽  
Jhonatan Orsolin

ABSTRACT The volatilization of ammonia (NH3) and nitrate leaching (NH3-) are the main processes of nitrogen (N) loss in the soil. The objective of the study was to evaluate N losses by NH3 volatilization and mineral N transformations in the soil with urea coated with poultry litter (urea + litter) compared with other sources of N, under two moisture conditions. The experiment was conducted in a controlled environment with a 5 x 2 factorial arrangement with four replicates, five N sources (urea, SuperN®, Kimcoat®, urea + litter and control without fertilizer) and two moisture contents [80 and 100% of field capacity (FC)]. The total volatilized NH3 did not differ between the sources, regardless of the soil moisture condition, ranging from 10.8 to 13.2% of the total N applied. The transformation of NH4+ into NH3- did not vary between the sources, except for the control, but it differed between soil moisture contents, with equilibrium estimated at 31 and 38 days, in the treatments with 80 and 100% FC, respectively. The urea + litter has N losses by NH3 volatilization and speed of transformation of the soil mineral N similar to those of the other sources, and can be used to substitute them.


Sign in / Sign up

Export Citation Format

Share Document