Douglas-fir soil C and N properties a decade after termination of urea fertilization

2001 ◽  
Vol 31 (12) ◽  
pp. 2225-2236 ◽  
Author(s):  
Peter S Homann ◽  
Bruce A Caldwell ◽  
H N Chappell ◽  
Phillip Sollins ◽  
Chris W Swanston

Chemical and microbial soil properties were assessed in paired unfertilized and urea fertilized (>89 g N·m–2) plots in 13 second-growth Douglas-fir (Pseudotsuga menziesii (Mirb.) Franco) stands distributed throughout western Washington and Oregon. A decade following the termination of fertilization, fertilized plots averaged 28% higher total N in the O layer than unfertilized plots, 24% higher total N in surface (0–5 cm) mineral soil, and up to four times the amount of extractable ammonium and nitrate. Decreased pH (0.2 pH units) caused by fertilization may have been due to nitrification or enhanced cation uptake. In some soil layers, fertilization decreased cellulase activity and soil respiration but increased wood decomposition. There was no effect of fertilization on concentrations of light and heavy fractions, labile carbohydrates, and phosphatase and xylanase activities. No increase in soil organic C was detected, although variability precluded observing an increase of less than ~15%. Lack of a regionwide fertilization influence on soil organic C contrasts with several site-specific forest and agricultural studies that have shown C increases resulting from fertilization. Overall, the results indicate a substantial residual influence on soil N a decade after urea fertilization but much more limited influence on soil C processes and pools.


2021 ◽  
Vol 18 (18) ◽  
pp. 5185-5202
Author(s):  
Juhwan Lee ◽  
Raphael A. Viscarra Rossel ◽  
Mingxi Zhang ◽  
Zhongkui Luo ◽  
Ying-Ping Wang

Abstract. Land use and management practices affect the response of soil organic carbon (C) to global change. Process-based models of soil C are useful tools to simulate C dynamics, but it is important to bridge any disconnect that exists between the data used to inform the models and the processes that they depict. To minimise that disconnect, we developed a consistent modelling framework that integrates new spatially explicit soil measurements and data with the Rothamsted carbon model (Roth C) and simulates the response of soil organic C to future climate change across Australia. We compiled publicly available continental-scale datasets and pre-processed, standardised and configured them to the required spatial and temporal resolutions. We then calibrated Roth C and ran simulations to estimate the baseline soil organic C stocks and composition in the 0–0.3 m layer at 4043 sites in cropping, modified grazing, native grazing and natural environments across Australia. We used data on the C fractions, the particulate, mineral-associated and resistant organic C (POC, MAOC and ROC, respectively) to represent the three main C pools in the Roth C model's structure. The model explained 97 %–98 % of the variation in measured total organic C in soils under cropping and grazing and 65 % in soils under natural environments. We optimised the model at each site and experimented with different amounts of C inputs to simulate the potential for C accumulation under constant climate in a 100-year simulation. With an annual increase of 1 Mg C ha−1 in C inputs, the model simulated a potential soil C increase of 13.58 (interquartile range 12.19–15.80), 14.21 (12.38–16.03) and 15.57 (12.07–17.82) Mg C ha−1 under cropping, modified grazing and native grazing and 3.52 (3.15–4.09) Mg C ha−1 under natural environments. With projected future changes in climate (+1.5, 2 and 5.0 ∘C) over 100 years, the simulations showed that soils under natural environments lost the most C, between 3.1 and 4.5 Mg C ha−1, while soils under native grazing lost the least, between 0.4 and 0.7 Mg C ha−1. Soil under cropping lost between 1 and 2.7 Mg C ha−1, while those under modified grazing showed a slight increase with temperature increases of 1.5 ∘C, but with further increases of 2 and 5 ∘C the median loss of TOC was 0.28 and 3.4 Mg C ha−1, respectively. For the different land uses, the changes in the C fractions varied with changes in climate. An empirical assessment of the controls on the C change showed that climate, pH, total N, the C : N ratio and cropping were the most important controls on POC change. Clay content and climate were dominant controls on MAOC change. Consistent and explicit soil organic C simulations improve confidence in the model's estimations, facilitating the development of sustainable soil management under global change.



1977 ◽  
Vol 7 (4) ◽  
pp. 641-647 ◽  
Author(s):  
R. van den Driessche ◽  
J. E. Webber

Monthly sampling of stem inner bark, roots, litter, humus, and mineral soil was carried out in six 0.1-ha plots in a 47-year-old Douglas fir (Pseudotsugamenziesii (Mirb.) Franco) stand for 1 year. Pairs of plots had received urea fertilization at the rates of 0, 224, and 448 kg nitrogen (N)/ha 4 years previously. Inner bark and roots were chemically analysed to determine concentrations of total N, soluble N, ninhydrin-positive compounds, monosubstituted guanidino amino compounds, arginine, and proline. Concentration of total N was determined in litter, humus, and mineral soil samples, and concentration of mineralizable N was also determined in humus and mineral soil.All sets of data showed an effect of season, but analysis of root soluble N, root guanidino compounds, root arginine, and litter total N were the most satisfactory for distinguishing differences in N level due to fertilizer treatments. For this purpose root sampling was best done in June and July, and litter sampling between January and May. Soluble N concentration was higher in inner bark than in roots, but arginine concentration was higher in roots than in inner bark. Root arginine concentration was high in winter and decreased to a low level in October before starting to accumulate again, suggesting it behaves as a N storage compound. Litter total N showed a decrease in concentration in July and August, followed by a recovery.



2020 ◽  
Author(s):  
Juhwan Lee ◽  
Raphael A. Viscarra Rossel ◽  
Zhongkui Luo ◽  
Ying Ping Wang

Abstract. We simulated soil organic carbon (C) dynamics across Australia with the Rothamsted carbon model (Rᴏᴛʜ C) under a framework that connects new spatially-explicit soil measurements and data with the model. Doing so helped to bridge the disconnection that exists between datasets used to inform the model and the processes that it depicts. Under this framework, we compiled continental-scale datasets and pre-processed, standardised and configured them to the required spatial and temporal resolutions. We then calibrated Rᴏᴛʜ C and run simulations to predict the baseline soil organic C stocks and composition in the 0–0.3 m layer at 4,043 sites in cropping, modified grazing, native grazing, and natural environments across Australia. The Rᴏᴛʜ C model uses measured C fractions, the particulate, humus, and resistant organic C (POC, HOC and ROC, respectively) to represent the three main C pools in its structure. The model explained 97–98 % of the variation in measured total organic C in soils under cropping and grazing, and 65 % in soils under natural environments. We optimised the model at each site and experimented with different amounts of C inputs to predict the potential for C accumulation in a 100-year simulation. With an annual increase of 1 Mg C ha−1 in C inputs, the model predicted a potential soil C increase of 13.58 (interquartile range 12.19–15.80), 14.21 (12.38–16.03), and 15.57 (12.07–17.82) Mg C ha−1 under cropping, modified grazing and native grazing, and 3.52 (3.15–4.09) Mg C ha−1 under natural environments. Soils under native grazing were the most potentially vulnerable to C decomposition and loss, while soils under natural environments were the least vulnerable. An empirical assessment of the controls on the C change showed that climate, pH, total N, the C:N ratio, and cropping were the most important controls on POC change. Clay content and climate were dominant controls on HOC change. Consistent and explicit soil organic C simulations improve confidence in the model's predictions, contributing to the development of sustainable soil management under global change.



2020 ◽  
Vol 8 (1) ◽  
pp. 1-8
Author(s):  
Refki Aulia Wiwaha ◽  
Syahrul Kurniawan

The Kali Kungkuk micro watershed which is located in the upper area of Brantas watershed, had experienced forest conversion to horticulture during the last fourth decades. Since the physiographic of Kali Kungkuk micro watershed is hilly, forest conversion to horticulture may result in soil nutrient stock changes. The research aimed to analyze soil nutrient stock from forest to horticulture land uses (i.e. apple orchard and vegetables) in the Kali Kungkuk micro watershed. The field research was conducted on three different land uses (i.e. vegetable land (PK), apple orchard (PA), and forest (PH)) and four land slope classes (i.e. slope 0-8% (K1), 8-15% (K2), 15-25% (K3), and > 25% (K4)), with three, replicates plots of each. Soil samples were collected at three different depths (0-10, 10-30, and 30- 50 cm) from each plot. The parameters measured included soil texture, bulk density, standing litter mass, canopy cover, basal area, soil organic carbon and total nitrogen. Data analysis was conducted with Linear Mixed Effect Models with a level of 5% and a further analysis of LSD test level of 5% as well as a correlation test between observational parameters. The results showed that differences in land use and slope affected to significant differences in the content of soil organic C and total N. In general, forests had higher soil C and N stocks as compared to other land uses (i.e. apple orchard and vegetables). Furthermore, soil organic C and total N was higher in the low slopes (i.e. 0-8%) and (8-15%) as compared to the high slopes (i.e. 15-25%) and (> 25%). The study found a positive correlation between soil nutrient stocks (i.e. C and N) and clay content. In contrast, soil C and N stock was negatively correlated with soil bulk density. Soil fertility degradation that occurs in the Kali Kungkuk micro watershed (i.e. apple orchard and vegetables) requires serious attention in soil management in order to ensure the sustainability of apple and vegetable production.



PeerJ ◽  
2020 ◽  
Vol 8 ◽  
pp. e8384
Author(s):  
Junyong Ma ◽  
Hairong Han ◽  
Xiaoqin Cheng

Forest soils sequester a large amount of carbon (C) and have a significant effect on the global C balance. Forests are commonly managed to maintain certain age structures but the effects of this management on soil C pools (kg C m−2) is still uncertain. We compared 40-year-old (1GF) and 24-year-old (2GF) plantations of Larix principis-rupprechtii in North China. Specifically, we measured environmental factors (e.g., soil temperature, moisture, and pH), the active C and nitrogen (N) pools (e.g., soil organic C, soil total N, dissolved organic C and N, microbial biomass C and N), and soil processes (e.g., C mineralization and microbial activity in different seasons) in five soil layers (0–50 cm, 10 cm for each soil layer) across the growing seasons in three 25 m × 25 m plots in each age class (1GF and 2GF). Findings indicated that the soil organic C pool in the older 1GF forest (12.43 kg C m−2) was significantly higher than 2GF forests (9.56 kg C m−2), and that soil temperature in 1GF forests was 9.8 °C, on average, 2.9% warmer than temperature in 2GF forests. The C lost as carbon dioxide (CO2) as a result of mineralization in the 2GF plots may partly explain the lower soil organic C pool in these younger forests; microorganisms likely drive this process.



2008 ◽  
Vol 32 (3) ◽  
pp. 1253-1260 ◽  
Author(s):  
Fabiano de Carvalho Balieiro ◽  
Marcos Gervasio Pereira ◽  
Bruno José Rodrigues Alves ◽  
Alexander Silva de Resende ◽  
Avílio Antonio Franco

In spite of the normally low content of organic matter found in sandy soils, it is responsible for almost the totality of cation exchange capacity (CEC), water storage and availability of plant nutrients. It is therefore important to evaluate the impact of alternative forest exploitation on the improvement of soil C and N accumulation on these soils. This study compared pure and mixed plantations of Eucalyptus grandis and Pseudosamanea guachapele, a N2-fixing leguminous tree, in relation to their effects on soil C and N stocks. The studied Planosol area had formerly been covered by Panicum maximum pasture for at least ten years without any fertilizer addition. To estimate C and N contents, the soil was sampled (at depths of 0-2.5; 2.5-5.0; 5.0-7.5; 7.5-10.0; 10.0-20.0 and 20.0-40.0 cm), in pure and mixed five-year-old tree plantations, as well as on adjacent pasture. The natural abundance 13C technique was used to estimate the contribution of the soil organic C originated from the trees in the 0-10 cm soil layer. Soil C and N stocks under mixed plantation were 23.83 and 1.74 Mg ha-1, respectively. Under guachapele, eucalyptus and pasture areas C stocks were 14.20, 17.19 and 24.24 Mg ha-1, respectively. For these same treatments, total N contents were 0.83; 0.99 and 1.71 Mg ha-1, respectively. Up to 40 % of the soil organic C in the mixed plantation was estimated to be derived from trees, while in pure eucalyptus and guachapele plantations these same estimates were only 19 and 27 %, respectively. Our results revealed the benefits of intercropped leguminous trees in eucalyptus plantations on soil C and N stocks.



1995 ◽  
Vol 25 (8) ◽  
pp. 1385-1396 ◽  
Author(s):  
T.A. Black ◽  
J.W. Harden

Four plots from a mixed conifer forest were similarly cleared, burned, and replanted at various times over 17 years; a plot logged 79 years before sampling was used as a control. The plots had similar slope (2 to 15%, midslope position), aspect (south to southeast), and soil type (Holland series: mesic Haploxeralf; a Gray Brown Luvisol in the Canadian classification system). Twenty sites at each plot were sampled volumetrically by horizon to 20 cm below the organic–mineral soil boundary. Samples were analyzed for bulk density, organic C, and total N. There was an initial loss (15%) of organic C from the soil within 1 to 7 years, likely the result of oxidation (burning and decomposition) and erosion. For 17 years of forest regrowth, the soil continued to lose C (another 15%), probably owing to decomposition of slash material and possibly erosion, despite the slight accumulation of new litter and roots. After 80 years of regrowth, rates of carbon accumulation exceeded rates of loss, but carbon storage had declined and was not likely to recover to preharvest levels. Timber harvest and site preparation dramatically altered soil C and N distribution, in which C/N ratios after site preparation were initially high throughout the upper 20 cm. Subsequently, C/N ratios became lower with depth and with recovery age. Although stocks of C and N varied considerably among the plots and did not change consistently as a function of recovery age, the C/N ratios did vary systematically with recovery age. We hypothesize that the amount of C ultimately stored in the soil at steady state depends largely on N reserves and potentials, which appear to vary with erosion, intensity of burning, and site treatment.



2006 ◽  
Vol 36 (12) ◽  
pp. 3148-3154 ◽  
Author(s):  
R EJ Boerner ◽  
T A Waldrop ◽  
V B Shelburne

We quantified the effects of three wildfire hazard reduction treatments (prescribed fire, thinning from below, and the combination of fire and thinning), and passive management (control) on mineral soil organic C, and enzyme activity in loblolly pine (Pinus taeda L.) forests on the Piedmont of South Carolina. Soil organic C was reduced by thinning, either alone or with prescribed fire, and this effect persisted through the fourth post-treatment year. Fire also resulted in reduced soil organic C, but not until several years after treatment. Soil C/N ratio initially increased after fire, either alone or with thinning, but this difference did not persist. The activities of three soil enzymes (acid phosphatase, chitinase, and phenol oxidase) in the upper mineral soil were quantified as measures of microbial activity. During the fourth post-treatment year we observed significant stimulation of all three enzyme systems as a result of thinning or thinning and burning. Although the patterns of variation in acid phosphatase and chitinase activity among treatments were similar during the first and fourth post-treatment years, the first-year treatment effects were not statistically significant. Given the management objective of utilizing these stands for timber production, the increased potential for rapid nutrient turnover offered by thinning gives this approach advantages over prescribed fire; however, management for maximum long-term storage of soil C may be better facilitated by prescribed fire.



2018 ◽  
Author(s):  
Jacqueline R. England ◽  
Raphael Armando Viscarra Rossel

Abstract. Maintaining or increasing soil organic carbon (C) is important for securing food production, and for mitigating greenhouse gas (GHG) emissions, climate change and land degradation. Some land management practices in cropping, grazing, horticultural and mixed farming systems can be used to increase organic C in soil, but to assess their effectiveness, we need accurate and cost-efficient methods for measuring and monitoring the change. To determine the stock of organic C in soil, one needs measurements of soil organic C concentration, bulk density and gravel content, but using conventional laboratory-based analytical methods is expensive. Our aim here is to review the current state of proximal sensing for the development of new soil C accounting methods for emissions reporting and in emissions reduction schemes. We evaluated sensing techniques in terms of their rapidity, cost, accuracy, safety, readiness and their state of development. The most suitable technique for measuring soil organic C concentrations appears to be vis–NIR spectroscopy and for bulk density active gamma-ray attenuation. Sensors for measuring gravel have not been developed, but an interim solution with rapid wet-sieving and automated measurement appears useful. Field-deployable, multi-sensor systems are needed for cost-efficient soil C accounting. Proximal sensing can be used for soil organic C accounting, but the methods need to be standardised and procedural guidelines need to be developed to ensure proficient measurement and accurate reporting and verification. This is particularly important if the schemes use financial incentives for landholders to adopt management practices to sequester soil organic C. We list and discuss the requirements for the development of new soil C accounting methods that are based on proximal sensing, including requirements for recording, verification and auditing.



2019 ◽  
Vol 10 (2) ◽  
pp. 233-255 ◽  
Author(s):  
Efrén López-Blanco ◽  
Jean-François Exbrayat ◽  
Magnus Lund ◽  
Torben R. Christensen ◽  
Mikkel P. Tamstorf ◽  
...  

Abstract. There is a significant knowledge gap in the current state of the terrestrial carbon (C) budget. Recent studies have highlighted a poor understanding particularly of C pool transit times and of whether productivity or biomass dominate these biases. The Arctic, accounting for approximately 50 % of the global soil organic C stocks, has an important role in the global C cycle. Here, we use the CARbon DAta MOdel (CARDAMOM) data-assimilation system to produce pan-Arctic terrestrial C cycle analyses for 2000–2015. This approach avoids using traditional plant functional type or steady-state assumptions. We integrate a range of data (soil organic C, leaf area index, biomass, and climate) to determine the most likely state of the high-latitude C cycle at a 1∘ × 1∘ resolution and also to provide general guidance about the controlling biases in transit times. On average, CARDAMOM estimates regional mean rates of photosynthesis of 565 g C m−2 yr−1 (90 % confidence interval between the 5th and 95th percentiles: 428, 741), autotrophic respiration of 270 g C m−2 yr−1 (182, 397) and heterotrophic respiration of 219 g C m−2 yr−1 (31, 1458), suggesting a pan-Arctic sink of −67 (−287, 1160) g Cm−2 yr−1, weaker in tundra and stronger in taiga. However, our confidence intervals remain large (and so the region could be a source of C), reflecting uncertainty assigned to the regional data products. We show a clear spatial and temporal agreement between CARDAMOM analyses and different sources of assimilated and independent data at both pan-Arctic and local scales but also identify consistent biases between CARDAMOM and validation data. The assimilation process requires clearer error quantification for leaf area index (LAI) and biomass products to resolve these biases. Mapping of vegetation C stocks and change over time and soil C ages linked to soil C stocks is required for better analytical constraint. Comparing CARDAMOM analyses to global vegetation models (GVMs) for the same period, we conclude that transit times of vegetation C are inconsistently simulated in GVMs due to a combination of uncertainties from productivity and biomass calculations. Our findings highlight that GVMs need to focus on constraining both current vegetation C stocks and net primary production to improve a process-based understanding of C cycle dynamics in the Arctic.



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