scholarly journals Soil organic carbon dynamics along a climatic gradient in a southern Appalachian spruce–fir forest

2007 ◽  
Vol 37 (7) ◽  
pp. 1161-1172 ◽  
Author(s):  
C.E. Tewksbury ◽  
H. Van Miegroet

A field study was conducted in a high-elevation spruce–fir ( Picea rubens Sarg. – Abies fraseri (Pursh.) Poir) forest in the Great Smoky Mountains National Park to assess the effect of temperature on soil C storage and dynamics. In eight plots along an elevation gradient (1500–1900 m), we measured soil temperature, forest floor and mineral soil C, litter decomposition, soil respiration, and forest floor mean residence time. Mean annual soil temperature and annual degree-days above 5 °C were inversely correlated with elevation. Total soil C (166–241 Mg·ha–1) showed no trend with elevation, while forest floor C accumulation (16.3–35.9 Mg·ha–1) decreased significantly with elevation. Carbon dynamics did not follow a consistent elevation pattern; however, the cooler upper elevations showed the lowest C turnover as indicated by the lowest needle decomposition rate (k = 0.0231·year–1) and the longest mean residence time of forest floor C (22 years). Mean annual CO2efflux from the soil (1020–1830 kg C·ha–1·year–1) was negatively correlated with mean annual soil temperatures and annual degree-days above 5 °C. This gradient study offers useful insights into C release patterns under future warming scenarios, and suggests that the highest elevation may be most susceptible to global warming.

2021 ◽  
Author(s):  
Han Lyu ◽  
Tetsuhiro Watanabe ◽  
Ruohan Zhong ◽  
Method Kilasara ◽  
Arief Hartono ◽  
...  

<p>Clarifying the controlling factors for soil organic carbon (SOC) stabilization is a primary issue in mitigating climate change. However, the mechanisms controlling soil carbon cycle are not well-understood, especially in tropical regions. Furthermore, the mechanisms are expected to differ between topsoil and subsoil. The objectives were to clarify the controlling factors for SOC pools partitioned by their stabilities, then to compare the differences in pools and controlling factors between topsoil and subsoil.</p><p>Both top (0–15 cm) and subsoil (20–40 cm) samples were collected at volcanic regions of Tanzania and Indonesia along an elevation gradient under mostly undisturbed vegetation (23 sites). A kinetic model, including labile, intermediate, and stable pools, was fitted to accumulative SOC mineralization curve obtained from 343-day incubation to determine the sizes of the labile and intermediate SOC pools (C<sub>L</sub> and C<sub>I</sub>) and their mean residence times, where the size of the stable SOC pool (C<sub>S</sub>) was measured as non-hydrolyzable carbon by fractionation. Correlation and path analyses were conducted to determine the controlling factors for each SOC pool, using the results of the model fitting and SOC fractionation and the data on climate, geochemistry, and biology (e.g., mean average temperature and precipitation, nanocrystalline mineral content (Al<sub>o</sub>+1/2Fe<sub>o</sub>), and microbial biomass, respectively).</p><p>The intermediate pool (56.2 ± 10.4% of SOC) predominantly contributed to the storage and stability of total SOC (10 to 157 g kg<sup>−1</sup>) for both topsoil and subsoil with the mean residence time of years to decades (3400 to 31500 days). For both topsoil and subsoil, Al<sub>o</sub>+1/2Fe<sub>o</sub> was strongly correlated with C<sub>I</sub> and C<sub>S</sub>, suggesting that organo-mineral complexation is a predominant factor that controls the intermediate and stable SOC pools, rather than soil pH or texture. Also, temperature negatively affected the sizes of all three pools, which indicates the low temperature retards the decomposition of all parts of SOC. The labile SOC pool was more controlled by biotic and climatic factors (i.e., microbial biomass and excess precipitation). Concerning differences between topsoil and subsoil, SOC was more in the intermediate than in the stable pool, and the effect of temperature on C<sub>S</sub> was more substantial in the subsoil. Moreover, Al<sub>o</sub>+1/2Fe<sub>o</sub> controlled the mean residence time of the intermediate SOC pool, indicating the stability of subsoil SOC that had a labile nature would be more dependent on nanocrystalline minerals.</p><p>While temperature widely influences all SOC pools, geochemical factors control more stable pools and total SOC storage, whereas biotic factors and moisture mainly alter relatively labile SOC pools. The subsoil SOC would be more sensitive to climate change than topsoil SOC. The findings helped to understand SOC stabilization mechanisms for both top and subsoils in tropical volcanic regions.</p>


1990 ◽  
Vol 20 (9) ◽  
pp. 1530-1535 ◽  
Author(s):  
Keith Van Cleve ◽  
Walter C. Oechel ◽  
John L. Hom

This paper reports results of a study designed to examine the control that soil temperature exerts on soil processes associated with nutrient flux, and in turn, on tree nutrition in interior Alaska black spruce ecosystems. Approximately 50 m2 of forest floor in a 140-year-old black spruce ecosystem, which had developed on permafrost, was heated to 8–10 °C above ambient temperature. This perturbation amounted to approximately a 1589 degree-day seasonal heat sum (above 0 °C), 1026 degree-days above the control total of 563 degree-days. The forest floor, surface 5 cm of mineral soil, and soil solution were compared with those of an adjacent control plot to evaluate the change in nutrient content and decomposition rate of the forest floor. The nutritional response to soil heating of current black spruce foliage also was evaluated. Soil heating significantly increased decomposition of the forest floor, principally because of an increase in biomass loss of the O21 layer. The increased decomposition resulted in greater extractable N and P concentrations in the forest floor, higher N concentrations in the soil solution, and elevated spruce needle N, P, and K concentrations for the experimental period. These results are discussed in light of the importance of soil temperature and other state factors that mediate ecosystem function.


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.


2011 ◽  
Vol 8 (2) ◽  
pp. 353-364 ◽  
Author(s):  
M. R. Hoosbeek ◽  
M. Lukac ◽  
E. Velthorst ◽  
A. R. Smith ◽  
D. L. Godbold

Abstract. Through increases in net primary production (NPP), elevated CO2 is hypothesized to increase the amount of plant litter entering the soil. The fate of this extra carbon on the forest floor or in mineral soil is currently not clear. Moreover, increased rates of NPP can be maintained only if forests can escape nitrogen limitation. In a Free atmospheric CO2 Enrichment (FACE) experiment near Bangor, Wales, 4 ambient and 4 elevated [CO2] plots were planted with patches of Betula pendula, Alnus glutinosa and Fagus sylvatica on a former arable field. After 4 years, biomass averaged for the 3 species was 5497 (se 270) g m−2 in ambient and 6450 (se 130) g m−2 in elevated [CO2] plots, a significant increase of 17% (P = 0.018). During that time, only a shallow L forest floor litter layer had formed due to intensive bioturbation. Total soil C and N contents increased irrespective of treatment and species as a result of afforestation. We could not detect an additional C sink in the soil, nor were soil C stabilization processes affected by elevated [CO2]. We observed a decrease of leaf N content in Betula and Alnus under elevated [CO2], while the soil C/N ratio decreased regardless of CO2 treatment. The ratio of N taken up from the soil and by N2-fixation in Alnus was not affected by elevated [CO2]. We infer that increased nitrogen use efficiency is the mechanism by which increased NPP is sustained under elevated [CO2] at this site.


1983 ◽  
Vol 13 (5) ◽  
pp. 747-766 ◽  
Author(s):  
Keith Van Cleve ◽  
Lola Oliver ◽  
Robert Schlentner ◽  
Leslie A. Viereck ◽  
C. T. Dyrness

This paper considers the productivity and nutrient cycling in examples of the major forest types in interior Alaska. These ecosystem properties are examined from the standpoint of the control exerted over them by soil temperature and forest-floor chemistry. We conclude that black spruce Piceamariana (Mill.) B.S.P. occupies the coldest, wettest sites which support tree growth in interior Alaska. Average seasonal heat sums (1132 ± 32 degree days (DD)) for all other forest types were significantly higher than those encountered for black spruce (640 ± 40 DD). In addition, black spruce ecosystems display the highest average seasonal forest-floor and mineral-soil moisture contents. Forest-floor chemistry interacts with soil temperature in black spruce to produce the most decay-resistant organic matter. In black spruce the material is characterized by the highest lignin content and widest C/N (44) and C/P (404) ratios. Across the range of forest types examined in this study, soil temperature is strongly related to net annual aboveground tree production and the annual tree requirement for N, P, K, Ca, and Mg. Forest floor C/N and C/P ratios are strongly related to annual tree N and P requirement and the C/N ratio to annual tree production. In all cases these controls act to produce, in black spruce, the smallest accumulation of tree biomass, standing crop of elements, annual production, and element requirement in aboveground tree components.


2005 ◽  
Vol 35 (9) ◽  
pp. 2118-2129 ◽  
Author(s):  
E S Kane ◽  
D W Valentine ◽  
E AG Schuur ◽  
K Dutta

The amount of soil organic carbon (SOC) in stable, slow-turnover pools is likely to change in response to climate warming because processes mediating soil C balance (net primary production and decomposition) vary with environmental conditions. This is important to consider in boreal forests, which constitute one of the world's largest stocks of SOC. We investigated changes in soil C stabilization along four replicate gradients of black spruce productivity and soil temperature in interior Alaska to develop empirical relationships between SOC and stand and physiographic features. Total SOC harbored in mineral soil horizons decreased by 4.4 g C·m–2 for every degree-day increase in heat sum within the organic soil across all sites. Furthermore, the proportion of relatively labile light-fraction (density <1.6 g·cm–3) soil organic matter decreased significantly with increased stand productivity and soil temperature. Mean residence times of SOC (as determined by Δ14C) in dense-fraction (>1.6 g·cm–3) mineral soil ranged from 282 to 672 years. The oldest SOC occurred in the coolest sites, which also harbored the most C and had the lowest rates of stand production. These results suggest that temperature sensitivities of organic matter within discrete soil pools, and not just total soil C stocks, need to be examined to project the effects of changing climate and primary production on soil C balance.


2004 ◽  
Vol 34 (3) ◽  
pp. 509-518 ◽  
Author(s):  
J Bauhus ◽  
T Vor ◽  
N Bartsch ◽  
A Cowling

Despite the importance of gaps in the dynamics and management of many forest types, very little is known about the medium- to long-term soil C and N dynamics associated with this disturbance. This study was designed to test the hypothesis that gap creation and lime application, a routine measure in many European forests to ameliorate soil acidity, lead to accelerated litter decomposition and thus a reduction in the forest floor and soil C and N pools. Four gaps were created in 1989 in a mature European beech (Fagus sylvatica L.) forest on acid soil with a moder humus, and lime (3 t dolomite·ha–1) was applied to two of these and surrounding areas. Litter and fine-root decomposition was measured in 1992–1993 and 1996–1998 using litterbags. Forest floor (L, F, and H layers) and mineral soil (0–40 cm) C and N pools were determined in 1989 and 1997. Eight years following silvicultural treatments, there was no change in C and N over the entire forest soil profile including forest floor. Reductions in the F and H layers in limed gaps were compensated for by increases in soil C and N in the surface (0–10 cm) mineral soil. Decomposition of F litter was significantly accelerated in limed gaps, leading to the development of a mull–moder, whereas gap creation alone had no effect on mass loss of F material in litterbags. Gap size disturbances in this acid beech forest appear to have minimal influences on soil C and N stocks. However, when combined with liming, changes in the humus form and vertical distribution of soil C and N may occur.


2013 ◽  
Vol 10 (1) ◽  
pp. 787-813 ◽  
Author(s):  
D. Zhou ◽  
S. Q. Zhao ◽  
S. Liu ◽  
J. Oeding

Abstract. Partial cutting, which removes some individual trees from a forest, is one of the major and widespread forest management practices that can significantly alter both forest structure and carbon (C) storage. Using 746 observations from 82 publications, we synthesized the impacts of partial cutting on three variables associated with forest structure (i.e. mean annual growth of diameter at breast height (DBH), basal area (BA), and volume) and four variables related to various C stock components (i.e. aboveground biomass C (AGBC), understory C, forest floor C, and mineral soil C). Results shows that the growth of DBH elevated by 112% after partial cutting, compared to the uncut control, while stand BA and volume reduced immediately by 34% and 29%, respectively. On average, partial cutting reduced AGBC by 43%, increased understory C storage by 392%, but did not show significant effects on C storages on forest floor and in mineral soil. All the effects on DBH growth, stand BA, volume, and AGBC intensified linearly with cutting intensity (CI) and decreased linearly with the number of recovery years (RY). In addition to the strong impacts of CI and RY, other factors such as climate zone and forest type also affected forest responses to partial cutting. The data assembled in this synthesis were not sufficient to determine how long it would take for a complete recovery after cutting because long-term experiments were rare. Future efforts should be tailored to increase the duration of the experiments and balance geographic locations of field studies.


2016 ◽  
Vol 46 (12) ◽  
pp. 1459-1473 ◽  
Author(s):  
Line Tau Strand ◽  
Ingeborg Callesen ◽  
Lise Dalsgaard ◽  
Heleen A. de Wit

Relationships between soil C and N stocks and soil formation, climate, and vegetation were investigated in a gridded database connected to the National Forest Inventory in Norway. For mineral soil orders, C and N stocks were estimated to be 11.1–19.3 kg C·m−2 and 0.41–0.78 kg N·m−2, respectively, declining in the following order: Gleysols > Podzols > Brunisols > Regosols. Organic peat-type soils stored, on average, 31.3 kg C·m−2 and 1.10 kg N·m−2, whereas shallow Organic folisols stored, on average, 10.2 kg C·m−2 and 0.34 kg N·m−2. For Norway’s 120 000 km2 of forest, the total of soil C stocks was estimated to be 1.83 Gt C, with a 95% CI of 1.71–1.95 Gt C. Podzolic soils comprise the largest soil group and store approximately 50% of the forest soil C. Sixty percent of the soil C stock in Podzolic soils was stored in the mineral soil, increasing with temperature and precipitation. Poorly drained soil types store approximately 47% of the total forest soil C in Norway. Soils with water saturation have large C stocks mainly in the forest floor, suggesting that they are more susceptible to forest management and environmental change. Soil C stocks under pine and spruce forests were similar, although pine forests had larger C stocks in the forest floor, while spruce forests had the highest C stocks in the mineral soil compartment. C stocks in the forest floor increase from dry to moist ground vegetation, while ground vegetation nutrient classes reflect better the C and N stocks in the mineral soil.


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%).


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