Prediction of organic carbon content in upland forest soils of Quebec, Canada

2002 ◽  
Vol 32 (5) ◽  
pp. 903-914 ◽  
Author(s):  
Sylvie Tremblay ◽  
Rock Ouimet ◽  
Daniel Houle

Soil organic carbon (C) is an important component of forest carbon pools and should be taken into account in sustainable forest management. However, there is a need to derive indicators for this attribute, as organic C content (Mg·ha–1) in forest soils is generally not available in Quebec survey data. Thus, we developed models to predict organic C accumulation in the forest floor and in mineral soils of upland forest soils (i.e., with forest floor thickness [Formula: see text]30 cm) using soil survey data as input variables. The best-fit model for predicting forest floor organic C content consisted of the explanatory variables forest floor thickness, latitude, and longitude. The model R2 was 0.76, and its CV was 28%. The second best-fit model, excluding geographical coordinates, included forest floor thickness and mean growing season precipitation as explanatory variables (R2 = 0.71, CV = 29.5%). The model for predicting mineral soil organic C content was composed of two submodels: (i) organic C concentration of a mineral horizon as a function of its colour and (ii) bulk density of that horizon as a function of its estimated C concentration (obtained from the former model). The R2 of the model for predicting organic C content in mineral soils was 0.57, and its CV was 29%. The models were used to predict organic C contents in 5547 pedons, dispersed throughout the commercial forest of Quebec and for which basic soil profile description data were available. It was then possible to evaluate and compare mean soil C accumulation in different forest stand types and to construct two maps of soil organic C accumulation in upland forest soils of southern Quebec. The results pointed out that forest floor thickness combined with mineral soil horizon colour, texture class, and pH would be useful sustainable forest management indicators of organic C accumulation in upland forest soils.

1996 ◽  
Vol 26 (8) ◽  
pp. 1353-1365 ◽  
Author(s):  
Bruce D. LaZerte ◽  
Lem Scott

A predominantly coniferous catchment on the Precambrian Shield had significantly more acid, base-poor, and Al-rich soil solutions than a predominantly deciduous catchment. Eight-year median depth profiles of the forest floor solutions revealed that ceramic tension lysimeters collected significantly higher levels of Al and Si, lower amounts of NO3−, and equal amounts of dissolved organic carbon than plastic zero-tension lysimeters. There was no significant difference between lysimeter types in the deeper mineral soils. NO3−, NH4+, K+, organic C, organic Al, Fe, and to a lesser extent Ca2+ and Mg2+ were more abundant in forest floor solutions than in the mineral soils. Inorganic Al, F−, Na+, and SO42− were more abundant in the mineral horizons, and Cl− was uniform throughout the profile. Calculations based on the Na profile and the weathering of plagioclase feldspars suggested that secondary Al and Si minerals were accumulating in the mineral soil. Long-term median inorganic Al concentrations followed the microcrystalline gibbsite solubility curve (−log(Al3+) = −9.2 + 3.0(pH); R2 = 0.97), and F− was closely correlated (R2 = 0.7). NO3−, NH4+, and K+ in the forest floor exhibited the strongest seasonal patterns, with peaks during the winter–spring snowmelt and late summer. Their levels increased severalfold in response to summer drought, but there was little response in the lower horizons. Apparently because of a decline in SO42− and possibly Ca2+ deposition, there was a long-term decline in Ca2+ and SO42− in the stream draining the PCl mineral horizons (approximately −2.1 ± 0.4 μequiv.•L−1•year−1), and a similar Ca2+ decline in the mineral soil solutions themselves. However, there was no change in pH or inorganic Al levels.


2000 ◽  
Vol 30 (7) ◽  
pp. 1034-1040 ◽  
Author(s):  
Friederike Lang ◽  
Martin Kaupenjohann

Molybdenum plays an important role in the nitrogen turnover of ecosystems. However, very little is known about Mo availability in forest soils. We measured the oxalate-extractable Mo concentrations of acid forest soils, the Mo, nitrate, phosphate, and sulfate fluxes from the organic forest floor into the mineral soil using resin tubes and the Mo concentrations of the tree needles at 28 different Norway spruce (Picea abies (L.) Karst.) sites in southern Germany. The supply of oxalate-extractable Mo varied from 51 to 3400 g·ha-1, with the lowest values occurring in sandstone-derived soils (370 ± 212 g·ha-1; mean ± SD). Molybdenum concentrations of current-year needles were in the range of 5 to 48 ng·g-1. The Mo needle concentrations and oxalate-extractable Mo of soils did not correlate. However, Mo fluxes (6-60 g·ha-1·a-1) from the organic forest floor into the mineral soils were correlated to needle concentrations and to the NO3 fluxes. We conclude that Mo turnover within forest ecosystems is governed by Mo plant availability of mineral soils as well as by plant Mo uptake. In addition, Mo cycling strongly affects Mo distribution within soil profiles and Mo fluxes out of the organic layer.


2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Mbezele Junior Yannick Ngaba ◽  
Ya-Lin Hu ◽  
Roland Bol ◽  
Xiang-Qing Ma ◽  
Shao-Fei Jin ◽  
...  

Abstract Soil C and N turnover rates and contents are strongly influenced by climates (e.g., mean annual temperature MAT, and mean annual precipitation MAP) as well as human activities. However, the effects of converting natural forests to intensively human-managed plantations on soil carbon (C), nitrogen (N) dynamics across various climatic zones are not well known. In this study, we evaluated C, N pool and natural abundances of δ13C and δ15N in forest floor layer and 1-meter depth mineral soils under natural forests (NF) and plantation forest (PF) at six sites in eastern China. Our results showed that forest floor had higher C contents and lower N contents in PF compared to NF, resulting in high forest floor C/N ratios and a decrease in the quality of organic materials in forest floor under plantations. In general, soil C, N contents and their isotope changed significantly in the forest floor and mineral soil after land use change (LUC). Soil δ13C was significantly enriched in forest floor after LUC while both δ13C and δ15N values were enriched in mineral soils. Linear and non-linear regressions were observed for MAP and MAT in soil C/N ratios and soil δ13C, in their changes with NF conversion to PF while soil δ15N values were positively correlated with MAT. Our findings implied that LUC alters soil C turnover and contents and MAP drive soil δ13C dynamic.


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.


2008 ◽  
Vol 20 (9) ◽  
pp. 1082-1089 ◽  
Author(s):  
Xuejun OUYANG ◽  
Guoyi ZHOU ◽  
Zhongliang HUANG ◽  
Cunyu ZHOU ◽  
Jiong LI ◽  
...  

2007 ◽  
Vol 37 (6) ◽  
pp. 1118-1133 ◽  
Author(s):  
Rock Ouimet ◽  
Sylvie Tremblay ◽  
Catherine Périé ◽  
Guy Prégent

We assessed the organic C stocks and inferred their changes in vegetation biomass, forest floor, and soil using a 50 year chronosequence of red pine ( Pinus resinosa Ait.) plantations established on postagricultural fields in southern Quebec, Canada. The data come from soil and tree field surveys carried out in the 1970s in 348 sites. Organic C concentrations were usually measured in three major mineral soil horizons; for the remaining soil horizons, they were estimated using pedotransfer functions. The effect of soil order, drainage, and texture was analysed. Over 22 years, organic C accumulation rates (Mg C·ha–1·year–1) were 1.66 ± 0.03 in vegetation biomass, 0.56 ± 0.07 in forest floor, 0.86 ± 0.47 in loamy soils (0–100 cm), and  –0.18 ± 0.24 in sandy soils (0–100 cm). The greater rate of C accumulation in loamy soils was due to the contribution of the 30–100 cm subsoil layer. The overall net accumulation of organic C in these plantation ecosystems was estimated to 51.4 ± 4.8 Mg C·ha–1 at 22 years. Soils of these plantations acted as a C sink in the first two decades, particularly in loamy soils compared with sandy soils, with no major differences among soil order or drainage.


2000 ◽  
Vol 80 (3) ◽  
pp. 507-514 ◽  
Author(s):  
Sylvain St-Laurent ◽  
Rock Ouimet ◽  
Sylvie Tremblay ◽  
Louis Archambault

Following the Rio and Kyoto protocols, forest sequestration of organic C (Corg) appears to be among the measures to reduce atmospheric C. In this context, we assessed the evolution of soils' reserves of Corg after complete whole-tree forest harvesting in the balsam fir–yellow birch forest of eastern Quebec. The experimental design consisted of eight plots in mature stands, and 10 plots in 7-, 12-, and 22-yr-old clearcuts in the "Seigneurie du Lac Métis", located 80 km south-east of Rimouski, Quebec, Canada. The soil type was an Orthic Humo-ferric Podzol. Major Corg losses occured in the forest floor of the 7-, 12- and 22-yr-old harvested plots compared with mature stands. The FH horizon of harvested plots showed a loss of 44% (−30.5 t ha−1) in dry weight and 13.5% (−62.1 g kg–1) in Corg content between 7 and 22-yr-old harvested plots. More than half the Corg content of the forest floor was lost in that time (−52% or −16.6 t ha−1). The Corg stock of the L horizon were lowered only for the 7-yr-old treatment (2.5 t ha−1) compared with mature stands (4.9 t ha−1). No significant differences in the Corg stocked in the first 30 m of the mineral soil were found between treatments. It appears that the forest floor of balsam fir–yellow birch stands has become a source of Corg for at least 22 yr after forest harvesting. Key words: Forest harvesting, soil, organic carbon, forest floor


1996 ◽  
Vol 26 (7) ◽  
pp. 1266-1272 ◽  
Author(s):  
W.Z. Huang ◽  
J.J. Schoenau

The purpose of this study was to characterize the quantity, distribution, and variance of water-soluble organic C (WSOC) in a soil under trembling aspen (Populustremuloides Michx.) in the southern boreal forest of Canada. WSOC was determined monthly from May to October 1994 in the forest floor horizons (L, F, H) and mineral soil (Ae) of an aspen stand in Prince Albert National Park, Saskatchewan. The concentration of WSOC varied considerably with profile depth, but varied little among the slope positions and aspects. The L horizon had the highest WSOC concentration (425–8690 mg•kg−1 ovendried soil), followed by the F, H, and Ae horizons. The concentration of WSOC in the Ae horizon was significantly related to the concentration in forest floor horizons above. Water-soluble organic C in the Ae horizon likely was derived from the overlying organic layer by leaching. In a laboratory incubation, the rate of WSOC release (the net result of release and uptake) during incubation decreased continuously over time, but in the field, the rate of WSOC release decreased slightly early in the growing season, but increased later in the season as new litter fall reached the forest floor. This indicates that litter fall is a major factor in the replenishment of WSOC in aspen forest stands.


1993 ◽  
Vol 23 (5) ◽  
pp. 956-963 ◽  
Author(s):  
K.M. Klingensmith ◽  
K. Van Cleve

Forest floors and mineral soils from early (open willow), middle (poplar–alder), and late (white spruce) floodplain primary successional stages were examined for nitrogen fixation and denitrification. The acetylene-reduction and acetylene-inhibition techniques were used separately and in combination to measure nitrogenase and denitrification activities, both in laboratory and field studies. In situ N2O production was undetectable at all sites and during all sampling periods. Denitrifying activity measured in the field with acetylene amendments was low to undetectable, except after a brief flood in the open willow stand when N2O production ranged from undetectable to 34 ng N•cm−2•h−1 within the newly deposited alluvium–old mineral soil interface. Intact core assays also had low to undetectable denitrification activities; the highest activities (259 ng N•g−1 h−1) were measured in the poplar–alder forest floor in the fall. Laboratory studies showed that potential denitrification enzyme activity (DEA) was also greatest in the poplar–alder forest floor (4332 ng N•g−1•h−1), once again occurring in the fall. In early and midsuccessional stages, the interactive effects of temperature, carbon, and NO3− limited denitrification, yet even with the addition of the limiting amendments, low to undetectable DEA was observed in mineral soils. The later white spruce successional stage also had low to undetectable DEA, increasing only with the addition of the full DEA media and independent of temperature changes. Nonsymbiotic nitrogenase activities were highly variable, ranging from undetectable to 30 ng N•cm−2•h−1. Highest activities were seen in the open willow, newly deposited alluvium–old mineral soil interface immediately after a flood and approximately 1 month after the flood on the newly deposited silt surface. Only the white spruce forest floor had measurable nonsymbiotic nitrogenase activity at all sampling times. Alder root nodule nitrogenase activity showed no significant differences between sampling periods. The estimated annual nitrogen fixation rate of 164 kg N•ha−1 for alder root nodules is a substantial N contribution to the alder stand and to the floodplain ecosystem in general.


2019 ◽  
Author(s):  
Axel Don ◽  
Christina Hagen ◽  
Erik Grüneberg ◽  
Cora Vos

Abstract. Most forest soils are characterised by a steep carbon gradient from the forest floor to the mineral soil, indicating that carbon is prevented from entry into the soil. Bioturbation can help incorporate litter-derived carbon into the mineral soil. Wild boar are effective at mixing and grubbing in the soil and wild boar populations are increasing in many parts of the world. In a six-year field study, we investigated the effect of wild boar bioturbation on the stocks and stability of soil organic carbon in two forest areas. Regular bioturbation mimicking grubbing by wild boar was performed artificially in 23 plots and the organic layer and mineral soil down to 15 cm depth were then sampled. No significant changes in soil organic carbon stocks were detected in the bioturbation plots compared with non-disturbed reference plots. However, around 50 % of forest floor carbon was transferred with bioturbation to mineral soil carbon and the stock of stabilised mineral-associated carbon increased by 28 %. Thus, a large proportion of the labile carbon in the forest floor was transformed into more stable carbon. Carbon saturation of mineral surfaces was not detected, but carbon loading per unit mineral surface increased by on average 66 % in the forest floor due to bioturbation. This indicates that mineral forest soils have non-used capacity to stabilise and store carbon. Transfer of aboveground litter into the mineral soil is the only rate-limiting process. Wild boar can help to speed up this process with their grubbing activity.


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