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iForest - Biogeosciences and Forestry

iForest - Biogeosciences and Forestry
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Controlling soil total nitrogen factors across shrublands in the Three Rivers Source Region of the Tibetan Plateau

iForest - Biogeosciences and Forestry, Volume 13, Issue 6, Pages 559-565 (2020)
doi: https://doi.org/10.3832/ifor3533-013
Published: Nov 29, 2020 - Copyright © 2020 SISEF

Research Articles

Alpine shrublands in the Three Rivers Source Region (TRSR) store substantial soil total nitrogen (N); however, limited information is available regarding its storage and controlling factors. To quantify the storage and controlling factors of soil total N stock, we analysed 66 soil profiles from samples obtained from 22 shrubland sites located across the TRSR on the Tibetan Plateau. Analytical methods, such as ordinary least squares regression, one-way analysis of variance, curve estimation, and variation partitioning were used to evaluate the effects of soil characteristics (soil organic carbon), vegetation characteristics (community types and ground cover of shrublands), climatic factors (mean annual temperature - MAT), and topographical features (slope) on soil N stock. Our results showed that soil N storage at a soil depth interval of 0-100 cm was 63.10 ± 27.41 Tg (Tg = 1012 g), with an average soil N stock of 2.44 ± 1.06 kg m-2 in the TRSR shrublands. Although the type of vegetation community had a small effect on soil N stock, the latter increased with increasing shrubland ground cover and soil organic carbon. However, soil N stock decreased with increasing topographical slope and MAT. Furthermore, changes in MAT primarily affected the N stock of topsoil. Among all the controlling factors, soil organic carbon explained most of the variation in the soil N stock. Considering the effects of global warming, an increase in MAT has decreased the soil N stock. Long-term monitoring of changes in soil N stock should be conducted to improve the precise estimation of soil N storage across the shrublands in the TRSR of the Tibetan Plateau.

Soil N Storage, Ground Cover, SOC, MAT, Alpine Shrublands, Tibetan Plateau

  Introduction 

Nitrogen (N) is an important limiting nutrient in northern ecosystems and is widely considered to be one of the most important elements in nutrient cycles ([1]). Within the N cycle in soils, significant greenhouse gases can be produced from ammonia (NH3) volatilisation and denitrification (NOx - [39]). As a key element, the storage of N in the soil is a basic input parameter for greenhouse gas, vegetation, and land surface models ([38]). Thus, studying soil N storage and its controlling factors is important to understand the relationship between carbon cycles in terrestrial ecosystems and global climate change ([43]).

Human activities, such as fertiliser use, industrial development, burning of biomass, expansion of agriculture, and deforestation have affected the N cycle ([37]) and even accelerated N deposition rate ([15]). Several studies have shown that global N deposition was 3-5 times higher in recent years than in the last century ([16]). In many regions, especially in Asia, N deposition is expected to increase faster ([6]). In China, over the past decades, total N deposition has not only significantly increased, but has also increased faster than that in Europe and the United States of America, even in the high-altitude region of the Tibetan Plateau ([12]). Accurate quantification of soil N stock is important for assessing the N capacity of soils to act as N sinks. Furthermore, uncertainties exist in the estimation of soil N stocks. Globally, researchers have estimated different soil N storages at 0-100 cm depths, for example, approximately 95 Pg ([34]) and 133-140 Pg ([3]). At a national scale, soil N storage in China (0-100 cm) was reported to be 7.4 Pg ([41]), which was lower than the previously estimated 8.29 Pg ([37]).

Soil characteristics ([1]), climatic factors ([19]), topography ([42]), and vegetation properties ([24]) have significant effects on soil N stock. Research has also demonstrated that soil depths, soil types ([41]), and soil parent materials ([1]) can affect soil N concentration and the over-soil N stock. Soil organic carbon (SOC) was observed to exhibit similar spatial distribution to soil N in the Loess Plateau of China ([11]) and eastern Rio Grande Plains, Texas, USA ([44]). Climatic changes have been observed to significantly affect nutrient dynamics, especially for N ([18]), and warmer, wetter climates contribute to soil N processes ([19]) including leaching and denitrification, which inevitably affect soil N storage.

Geomorphic disturbances and terrain characteristics ([33]) have also been demonstrated to affect soil N. Topography, including slope, has been found to play an important role in shaping microclimate environments, resulting in different temperatures and moisture levels, thus affecting the distribution of plant communities and various soil processes ([2]). However, topographical slope has also been found to significantly impact soil erosion ([4]), thus affecting soil N. This demonstrates that topographical factors play an important role in predicting soil N storage, and ignoring topographical effects increases the uncertainty of estimating soil N stock, especially in mountain regions ([42]).

In Mediterranean regions, vegetation types, including native and reforested plants, have also been found to affect soil N storage ([20]). However, the extensive heterogeneity found in soils has made vegetation types poor predictors of soil N stock ([37]). Specifically, soil N in the forest and woodlands of northern China was 14% higher than that in the wetlands. In contrast, soil N in the wetlands was found to be more than twice that in the forest and woodlands of southern China ([37]).

On the Tibetan Plateau, the following factors affect the soil N storage: yak grazing in the alpine meadows ([25]), soil characteristics, such as paedogenesis and physicochemical parameters in the alpine meadows ([26]), and different land cover types, including alpine wet meadows, alpine deserts, alpine steppes, alpine meadows, and barren lands ([43]). However, less attention has been paid to the shrublands of the Tibetan Plateau ([30]). It has been demonstrated that the mean annual temperature (MAT), instead of mean annual precipitation (MAP), primarily affects the soil N stock at a soil depth interval of 0-30 cm in the alpine shrublands of the Tibetan Plateau ([30]). However, previous research on the effects of climatic factors on soil N stock has only focused on topsoil (0-30 cm), while the response of soil N stock to increasing MAT in deeper soils, such as at 0-100 cm, remains unknown in these shrublands. Therefore, other factors affecting soil N stock in these shrublands should be studied.

Although uncertainties in the estimation of global N stocks usually exist, regional evaluations increase the precision of estimates ([41]). At a regional scale, the Three Rivers Source Region (TRSR) is distributed across the interiors of the Tibetan Plateau ([21]). So far, soil N storage has not been estimated in the TRSR. Regarding global warming, the TRSR has not only experienced climatic changes, but the changes experienced here were also greater than those experienced in other regions ([21]). It has been demonstrated that MAT has increased by 1.5 °C in the last 40 years ([35]), which will change the soil N stock ([24]). In this study, our aim was to evaluate the soil N storage across the shrublands of the TRSR and examine the factors controlling it. We tested the following hypotheses: (1) soil characteristics (such as SOC), geographic conditions (such as slope), and vegetation characteristics (including different dominant community types and ground cover of shrublands) can not only shape soil N stock, but also explain most variations in the soil N stock across the shrublands of the TRSR; (2) the effects of MAT on soil N stock are concentrated in the topsoil and soil N stock at depths of 0-100 cm is relatively insensitive to the changes in MAT.

  Materials and methods 

Study area

The study area was situated between latitudes 31.65 °N to 37.02 °N and longitudes 89.40 °E to 102.45 °E. The TRSR, also known as the “water tower of China” due to it consisting mainly of the Lancang (Mekong), Yellow, and Yangtze rivers, is situated in the central Tibetan Plateau which has the highest altitude, largest area, and most crowded distribution of rivers, lakes, and glaciers worldwide ([35]). Hence, despite the fragile ecological environment, the TRSR performs significant functions as an ecological security barrier for the Tibetan Plateau ([21]). Therefore, a nature reserve was established on the TRSR in 2000. Due to its unique geographical position and rich biodiversity, a Chinese national park was established in the TRSR in 2019. This upgrade from nature reserve to national park implied stricter management in the TRSR, ensuring less human disturbance. Alpine shrublands, a significant biome in the TRSR, is dominated by woody plants, such as Sibiraea laevigata, Potentilla fruticose, Rhododendron capitatum, and R. thymifolium, and many herbs, including Kobresia capillifolia, Leymus secalinus, Stipa purpurea, and K. parva. The main soil types in the region are leptosols, calcisols, chernozems, and cambisols, based on the soil classification system of the Food and Agriculture Organization (FAO) of the United Nations ([28]).

The climate of the TRSR represents a typical continental plateau climate ([10]). The mean altitude is 4000 m a.s.l., while the MATs and MAPs in the study area range from -5.6 to 3.8 °C and from 262 to 773 mm, respectively ([35]). Like the Tibetan Plateau, the TRSR is moving toward a warmer and wetter climate ([35]). Specifically, the MAT in the TRSR has been increasing by up to 0.27-0.33 °C every decade ([35]). Furthermore, MAP has also been increasing in the TRSR by up to 1.35 mm year-1 ([35]).

Field survey and laboratory measurements

To estimate the soil N stock in the alpine shrublands of the TRSR, a total of 66 soil profiles were systematically sampled from 22 typical sites in the shrublands from July to August from 2011 to 2013 (Fig. 1). Field surveys were conducted following the method prescribed by the Technical Manual Writing Group of the Ecosystem Carbon Sequestration Project ([9]). First, we conducted a preliminary survey of potential study sites based on the 1:1.000.000 scale vegetation atlas of China (Fig. 1). Afterwards, we confirmed the representativeness of the selected sites in the field. These selected sites had to satisfy two requirements: (i) the dominant community of shrublands should be larger than 1oo m2; and (ii) the site should have a relatively even distribution of habitat, species composition, and community structure ([9]). At each site, geographical conditions, such as slope, were determined using a geological compass (DQY-1A®, Optical Instrument Company, Haerbin, China), and three 5 × 5 m plots were identified. The distance between them was never less than 5 m or further than 50 m. Primary vegetation characteristics, such as the ground cover of woody plants and dominant woody species were visually estimated and recorded in each plot. At each plot, a soil profile (1 m long × 1.5 m wide × 1 m deep) was dug for the collection of samples at different depths (0-10, 10-20, 20-30, 30-50, 50-70, and 70-100 cm). Three sub-samples were collected using a standard 100 cm3 cylindrical container (height: 50 mm; diameter: 50.5 mm) for each depth and then mixed to form one composite sample per plot. The sample was dried at 105 °C for 24 h in the lab and then gravimetrically weighed. The soil bulk density of each sampled horizon was calculated as the ratio between the dry weight and total volume. Soil samples were then sieved at 2.0 mm. SOC was measured through wet oxidation following the Walkley-Black method, and organic matter was oxidised by adding sulphuric acid to potassium dichromate. Total soil N was measured through dry combustion using an elemental analyser (2400 CHNS/O® elemental analyser, Perkin-Elmer, Waltham, MA, USA). The temperatures for combustion and reduction were set to 950 °C and 640 °C, respectively.

Fig. 1 - The distribution of 22 sampling sites in the shrublands of the Three Rivers Source Region shown on a 1:1.000.000 scale background vegetation map ([7]).

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Climate data

To analyse the effects of climatic factors on soil N stock, the MAT data for each site were obtained from the WorldClim database (⇒ http:/­/­www.­worldclim.­org/­), with a spatial resolution of 1 × 1 km ([14]).

Data analysis

To determine the soil N stock and storage (their results and corresponding standard deviations using the 22 sites) at each soil depth, the following formulas were used (eqn. 1, eqn. 2).

\begin{equation} ND_{i} =\sum_{i=1}^{n}T_{i} \cdot N_{i} \cdot BD_{i} \cdot {\frac{1-C_{i}}{100}} \end{equation}
\begin{equation} NS_{i} =ND_{i} \cdot Area \end{equation}

where ND is the soil N stock (kg N m-2), Ti is the soil thickness (cm), Ni is the total N content (g kg-1), BDi is the bulk density (g cm-3), and Ci is the volume percentage of the fraction > 2 mm in layer i (cm). In eqn. 2, NSi is the soil N storage at layer i (cm), and Area is the area of shrublands across the TRSR.

The effects of MAT, SOC, and topographical slope of the shrublands on soil N stock were determined using ordinary least squares regression. Curve estimation was used to estimate the relationship between the ground cover of shrublands and soil N stock. Normality and homogeneity of variance were satisfied, and one-way analysis of variance (ANOVA) was used to compare the differences between various dominant community types. These analyses were performed using SPSS® v. 22.0 (IBM Corporation, Armonk, NY, USA) and the graphs were drawn using Origin® 2017 (OriginLab, Northampton, MA, USA). Variables that did not significantly contribute to the soil N stock were excluded from the variation partitioning analysis. The variation in soil N stock at depths of 0-30, 30-50, and 50-100 cm layers was partitioned using four explanatory factors that included SOC, slope, ground cover, MAT, and their combined effects. This analysis was performed using the “vegan” R software package ([36]).

  Results 

Storage, stock, and content of soil N in TRSR shrublands

The soil N storage in the TRSR shrublands was 63.10 ± 27.41 Tg at 0-100 cm soil depth interval, with an average soil N stock of 2.44 ± 1.06 kg m-2 (Tab. 1). The soil N content decreased with increasing soil depth and at the soil depth intervals of 0-10, 10-20, 20-30, 30-50, 50-70, 70-100 cm, it was found to be 6.44 ± 1.83, 5.23 ± 1.25, 4.25 ± 1.44, 3.32 ± 1.47, 2.68 ± 1.54, and 2.34 ± 1.93 g kg-1, respectively (Fig. 2).

Tab. 1 - Stock and storage of soil nitrogen (N) from soil surface to a depth of 100 cm in the shrublands of the Three Rivers Source Region. The results of soil N storage are shown as mean values ± standard deviation (SD).

Soil depth
(cm)
Soil N stock (kg m-2) Soil N storage
(Tg)
Min Max Mean SD
0-10 0.14 0.79 0.40 0.17 10.43 ± 4.44
0-20 0.35 1.45 0.80 0.28 20.78 ± 7.35
0-30 0.45 1.87 1.14 0.38 29.44 ± 9.72
0-50 0.61 2.69 1.64 0.54 42.40 ± 14.02
0-70 0.61 3.58 2.02 0.75 52.22 ± 19.39
0-100 0.61 4.72 2.44 1.06 63.10 ± 27.41

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Fig. 2 - Soil nitrogen (N) content at different soil depths across the shrublands of the Three Rivers Source Region.

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Factors controlling soil N stock in TRSR shrublands

SOC significantly affected soil N stock (Fig. 3). Specifically, soil N stock increased with SOC at soil depth intervals of 0-30 cm (Fig. 3A), and similar observations were made at soil depth intervals of 0-50 (Fig. 3B) and 0-100 cm (Fig. 3C).

Fig. 3 - Relationship between soil organic carbon (SOC) and soil nitrogen (N) stock in the shrublands of the Three Rivers Source Region at the soil depth intervals of (A) 0-30 cm, (B) 0-50 cm, and (C) 0-100 cm.

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Slope was also found to significantly affect soil N stock (Fig. 4). However, contrary to the relationship between SOC and soil N density, soil N stock decreased with increasing slope at the soil depth interval of 0-30 cm (Fig. 4A), and similar observations were made at depth intervals of 0-50 (Fig. 4B) and 0-100 cm (Fig. 4C).

Fig. 4 - Relationship between slope and soil nitrogen (N) stock in the shrublands of the Three Rivers Source Region at the soil depth intervals of (A) 0-30 cm, (B) 0-50 cm, and (C) 0-100 cm.

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The ground cover of shrublands can significantly stimulate the accumulation of soil N stock; indeed, it was observed to increase with ground cover at all soil depth intervals of 0-30 (Fig. 5A), 0-50 (Fig. 5B), and 0-100 cm (Fig. 5C).

Fig. 5 - Relationship between ground cover and soil N stock in the shrublands of the Three Rivers Source Region at the soil depth intervals of (A) 0-30 cm, (B) 0-50 cm, and (C) 0-100 cm.

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Soil N stock differences were observed for different shrubland community types, especially for P. fruticose and S. laevigata (Fig. 6). However, these differences were not significant (p > 0.05) according to the ANOVA results.

Fig. 6 - Relationship between vegetation types and soil N stock in the shrublands of the Three Rivers Source Region at the soil depth intervals of (A) 0-30 cm, (B) 0-50 cm, and (C) 0-100 cm. The solid black squares and error bars represent the mean of each measurement and corresponding standard deviations, respectively.

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Soil N stock was found to significantly decrease with increasing MAT (p < 0.05) at soil depth intervals of 0-30 (Fig. 7A) and 0-50 cm (p < 0.05 - Fig. 7B). However, a decreasing trend was not observed at soil depth intervals of 0-100 cm (p > 0.05 - Fig. 7C), which supported the hypothesis that the effects of MAT on soil N stock were concentrated in the topsoil, with deeper soils having a small effect.

Fig. 7 - Relationships between mean annual temperature (MAT) and soil nitrogen (N) stock in the shrublands of the Three Rivers Source Region at the soil depth intervals of (A) 0-30 cm, (B) 0-50 cm, and (C) 0-100 cm.

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Variables, such as slope, ground cover, SOC, and MAT, can significantly affect soil N stock at soil depth intervals of 0-30 and 0-50 cm; thus, these variables were selected to conduct variation partitioning analyses. Considering that the effect of MAT on soil N stock was insignificant at the soil depth interval of 0-100 cm, it was not included in the variation partitioning analyses for this depth interval. The results showed that the soil N stock was effectively explained by the selected variable, supporting the hypothesis. The amount of variation captured by all selected factors was 94.52%, 94.71%, and 94.31% for soil N stock at soil depth intervals of 0-30, 0-50, and 0-100 cm, respectively (Fig. 8). Individual SOC explained the most variations in the soil N stock for up to 68.54%, 63.94%, and 58.16% at soil depth intervals of 0-30, 0-50, and 0-100 cm, respectively (Fig. 8).

Fig. 8 - Results of variation partitioning analysis for soil nitrogen (N) stock at the soil depth intervals of in (A) 0-30 cm, (B) 0-50 cm, and (C) 0-100 cm across the shrublands of the Three Rivers Source Region. Variation partitioning analysis consists of explained variation, including effects of slope, ground cover, soil organic carbon (SOC), mean annual temperature (MAT), and their joint effects, and unexplained variations.

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  Discussion 

Relationship between SOC and soil N stock

Soil N stock was observed to increase with increasing SOC at all soil depth intervals of 0-30, 0-50, and 0-100 cm across the shrublands of the TRSR (Fig. 3). Similar observations have been made for the Loess Plateau ([11]). It has been demonstrated that N in soil is mainly determined by the decomposition and accumulation of soil organic matter ([44], [11]), which corresponds with the positive correlation observed between soil N stock and SOC.

In the TRSR, SOC has been demonstrated to contribute to a potential sink ([32]). Considering that and the positive correlation observed between SOC and soil N stock, a potentially increasing soil N can be inferred in future.

Relationship between soil N stock and slope

Variations in topography can result in different microclimates, inducing different plant growth and soil properties ([20]). It has been demonstrated that, although slope does not directly affect soil N storage in the grasslands of northern China, it can affect factors such as soil pH and bulk density, which can limit soil N storage ([42]). In this study, soil N stock was found to decrease with increasing slope. A steep slope can lead to soil erosion, which can significantly damage the environment and result in the loss of finer soil particles with higher N stock ([5]). Therefore, soil N stock was observed to decrease with increasing slope across the shrublands of the TRSR.

The negative relationship between soil N stock and slope indicated that conservation of soil by revegetation or reduced grazing to restrain soil erosion is necessary to maintain soil fertility ([13]).

Relationship among vegetation type, ground cover, and soil N stock

The amount of soil N storage is related to biotic processes, including decomposition of organic matter and productivity of plants ([34], [3]). Hence, vegetation type significantly affects soil N distribution ([41]). However, some studies have indicated that vegetation type is a poor predictor of soil N stock in China ([37]), consistent with our finding that the effects of different dominant shrubland communities on soil N stock were small in the TRSR. Similarly, in temperate and boreal forests, vegetation types have been found to have only a small impact on soil N storage ([24]). This difference could be due to high soil heterogeneity ([37]), which indicates that regional research on factors controlling soil N stock is significant for understanding terrestrial N cycles.

Higher ground cover of shrublands can stimulate the accumulation of soil N storage in the shrublands of the TRSR. Increased ground cover is derived from a growing shrubland canopy, which can stimulate more litter input to soil ([8]), thus increasing soil N stock. It has been demonstrated that climatic changes increase the ground cover of shrublands at high latitudes ([29]) and arctic and alpine regions ([27]), indicating that an increase in soil N storage may occur in the future ([23]).

Relationship between soil N stock and MAT

Increasing temperatures can accelerate microbial metabolism, which can contribute to gaseous losses by denitrification and volatilisation, decreasing the soil N stock ([17]). An increase in plant growth in the shrublands of the TRSR ([31]) has also contributed to the uptake of nutrients by plant roots, decreasing the soil N stock ([17]). However, it should be noted that in cold and wet regions, low temperatures generally limit plant growth ([40]). An increasing MAT has been demonstrated to stimulate aboveground biomass in the shrublands of the TRSR ([31]). Thus, more litter is transferred to the soil as one of the primary input resources ([24]), which aids in increasing the soil N stock. The effects of limited accumulation of N may exceed the positive effects on soil N stock, resulting in a negative relationship between MAT and soil N stock.

It has been found that soil N stock at soil depth intervals of 0-30 cm decreases with increasing MAT in the alpine shrublands of the Tibetan Plateau ([30]). Furthermore, this study demonstrated that soil N stock at a soil depth of 0-100 cm was independent of MAT, which showed that the soil N stock in deeper soils, such as at 50-100 cm depth, was less affected by MAT in the shrublands of the TRSR.

Amid the growing effects of global warming, MAT has been increasing by 1.5 °C in the TRSR ([35]). Considering only the negative relationship between temperature and soil N stock (Fig. 7), soil N storage was found to decrease. However, N dioxides have been anthropogenically emitted and may increase further ([22]). Further, global warming not only affects plant growth but also shifts plant species across the tundra ecosystem ([40]), changing the nutrient cycle. Therefore, long-term monitoring of changes in soil N stock is necessary to improve the precision of N storage estimation across the shrublands of the TRSR.

Controlling factors of soil N stock

The controlling factors of soil N stock in the shrublands can explain most soil N stock variables, with the unexplained variations being only 5.48%, 5.29%, and 5.69% at soil depth intervals of 0-30, 0-50, and 0-100 cm, respectively (Fig. 8), indicating that the factors controlling soil characteristics ([1]), topography ([42]), vegetation properties ([24]), and climatic factors ([19]) significantly affected the soil N stock. The dominant variable that determined the soil N stock was SOC across the shrublands of the TRSR. The individually explained variable of soil N stock from SOC was as high as 68.54%, 63.94%, and 58.16% at soil depth intervals of 0-30, 0-50, and 0-100 cm, respectively (Fig. 8), which indicated that SOC was a robust factor controlling the soil N stock in the shrublands of the TRSR.

  Conclusions 

Across the shrublands in the TRSR, total soil N storage at the soil depth interval of 0-100 cm was 63.10 ± 2 7.41 Tg and the average soil N stock was 2.44 ± 1.06 kg m-2. Increasing the ground cover of shrublands stimulated soil N accumulation. However, MAT and topographical slope were negatively related to soil N stock. Furthermore, the effect of MAT on soil N stock was concentrated on the topsoil. Most soil N stock variations were explained by climatic factors, soil characteristics, topography, and vegetation type in the TRSR, with SOC explaining the largest variation. In the global climate change scenarios, long-term monitoring of changes in soil N stock is necessary to improve the estimation of soil N stock across the shrublands of the TRSR in the Tibetan Plateau.

  Acknowledgements 

We thank Zebing Zhong, Wenzhu Song, Hechun Liu, Changbin Li, Yi Ning and Feng Xiong for facilitating our field surveys on the Tibetan Plateau and for their laboratory assistance. This study was funded by the National Key Research and Development Program of China (2019YFC0507404), the National Program on Basic Work Project of China (2015FY11030001-5), Natural Science Foundation of Qinghai (2019-ZJ-910), Qinghai Province International Exchange and Cooperation Project (2019-HZ-807), and the Strategic Priority Research Program of CAS (XDA0505030304).

  References

(1)
Augusto L, Achat DL, Jonard M, Vidal D, Ringeval B (2017). Soil parent material a major driver of plant nutrient limitations in terrestrial ecosystems. Global Change Biology 23: 3808-3824.
CrossRef | Gscholar
(2)
Bale CL, Williams JB, Charley JL (1998). The impact of aspect on forest structure and floristics in some Eastern Australian sites. Forest Ecology and Management 110: 363-377.
CrossRef | Gscholar
(3)
Batjes NH (1996). Total carbon and nitrogen in the soils of the world. European Journal of Soil Science 47: 151-163.
CrossRef | Gscholar
(4)
Cardinale BJ, Wright JP, Cadotte MW, Carroll IT, Hector A, Srivastava DS, Loreau M, Weis JJ (2007). Impacts of plant diversity on biomass production increase through time because of species complementarity. Proceedings of the National Academy of Sciences USA 104: 18123-18128.
CrossRef | Gscholar
(5)
Carroll C, Merton L, Burger P (2000). Impact of vegetative cover and slope on runoff, erosion, and water quality for field plots on a range of soil and spoil materials on central Queensland coal mines. Soil Research 38: 313-328.
CrossRef | Gscholar
(6)
Chen D, Li J, Lan Z, Hu S, Bai Y, Niu S (2016). Soil acidification exerts a greater control on soil respiration than soil nitrogen availability in grasslands subjected to long-term nitrogen enrichment. Functional Ecology 30: 658-669.
CrossRef | Gscholar
(7)
Chinese Academy of Science (2001). Vegetation atlas of China. Science Press, Beijing, China.
Gscholar
(8)
Cornelissen JH, Van Bodegom PM, Aerts R, Callaghan TV, Van Logtestijn RS, Alatalo J, Stuart Chapin F, Gerdol R, Gudmundsson J, Gwynn-Jones D (2007). Global negative vegetation feedback to climate warming responses of leaf litter decomposition rates in cold biomes. Ecology Letters 10: 619-627.
CrossRef | Gscholar
(9)
Ecosystem Carbon Sequestration Project (2015). Observation and investigation for carbon sequestration in terrestrial ecosystems. Technical Manual Writing Group of Ecosystem Carbon Sequestration Project, Science Press, Beijing, China, pp. 153-155.
Gscholar
(10)
Fan J, Shao Q, Liu J, Wang J, Harris W, Chen Z, Zhong H, Xu X, Liu R (2010). Assessment of effects of climate change and grazing activity on grassland yield in the Three Rivers Headwaters Region of Qinghai-Tibet Plateau, China. Environmental Monitoring and Assesment 170: 571-584.
CrossRef | Gscholar
(11)
Fang Z, Li D, Jiao F, Yao J, Du H (2019). The latitudinal patterns of leaf and soil C:N:P stoichiometry in the Loess Plateau of China. Frontiers in Plant Science 10: 85.
CrossRef | Gscholar
(12)
Han Y, Dong S, Zhao Z, Sha W, Li S, Shen H, Xiao J, Zhang J, Wu X, Jiang X, Zhao J, Liu S, Dong Q, Zhou H, Yeomans JC (2019). Response of soil nutrients and stoichiometry to elevated nitrogen deposition in alpine grassland on the Qinghai-Tibetan Plateau. Geoderma 343: 263-268.
CrossRef | Gscholar
(13)
He N, Yu Q, Wu L, Wang Y, Han X (2008). Carbon and nitrogen store and storage potential as affected by land-use in a Leymus chinensis grassland of northern China. Soil Biology and Biochemistry 40: 2952-2959.
CrossRef | Gscholar
(14)
Hijmans RJ, Cameron SE, Parra JL, Jones PG, Jarvis A (2005). Very high resolution interpolated climate surfaces for global land areas. International Journal of Climatology 25: 1965-1978.
CrossRef | Gscholar
(15)
Holland EA, Braswell BH, Sulzman J, Lamarque JF (2005). Nitrogen deposition onto the United States and western Europe: synthesis of observations and models. Ecological Application 15: 38-57.
CrossRef | Gscholar
(16)
Janssens IA, Dieleman W, Luyssaert S, Subke JA, Reichstein M, Ceulemans R, Ciais P, Dolman AJ, Grace J, Matteucci G, Papale D, Piao SL, Schulze ED, Tang J, Law BE (2010). Reduction of forest soil respiration in response to nitrogen deposition. Nature Geoscience 3 (5): 315-322.
CrossRef | Gscholar
(17)
Kulkarni MV, Groffman PM, Yavitt JB, Goodale CL (2015). Complex controls of denitrification at ecosystem, landscape and regional scales in northern hardwood forests. Ecological Modelling 298: 39-52.
CrossRef | Gscholar
(18)
LeBauer DS, Treseder KK (2008). Nitrogen limitation of net primary productivity in terrestrial ecosystems is globally distributed. Ecology 89: 371-379.
CrossRef | Gscholar
(19)
Liu Y, Wang C, He N, Wen X, Gao Y, Li S, Niu S, Butterbach-Bahl K, Luo Y, Yu G (2017). A global synthesis of the rate and temperature sensitivity of soil nitrogen mineralization: latitudinal patterns and mechanisms. Global Change Biology 23: 455-464.
CrossRef | Gscholar
(20)
Lozano-García B, Parras-Alcántara L, Brevik EC (2016). Impact of topographic aspect and vegetation (native and reforested areas) on soil organic carbon and nitrogen budgets in Mediterranean natural areas. Science of the Total Environment 544: 963-970.
CrossRef | Gscholar
(21)
Luo C, Wang J, Liu M, Liu Z (2014). Analysis on the change of grassland coverage in the Source Region of Three Rivers during 2000-2012. IOP Conference Series: Earth and Environmental Science 17: 012062.
CrossRef | Gscholar
(22)
Lü C, Tian H (2007). Spatial and temporal patterns of nitrogen deposition in China: Synthesis of observational data. Journal of Geophysical Research - Atmosphere 112: D22S05.
CrossRef | Gscholar
(23)
Marty C, Houle D, Gagnon C (2015). Variation in stocks and distribution of organic C in soils across 21 eastern Canadian temperate and boreal forests. Forest Ecology and Management 345: 29-38.
CrossRef | Gscholar
(24)
Marty C, Houle D, Gagnon C, Courchesne F (2017). The relationships of soil total nitrogen concentrations, pools and C:N ratios with climate, vegetation types and nitrate deposition in temperate and boreal forests of eastern Canada. Catena 152: 163-172.
CrossRef | Gscholar
(25)
Ma W, Ding K, Li Z (2016). Comparison of soil carbon and nitrogen stocks at grazing-excluded and yak grazed alpine meadow sites in Qinghai-Tibetan Plateau, China. Ecological Engineering 87: 203-211.
CrossRef | Gscholar
(26)
Mu C, Zhang T, Zhang X, Cao B, Peng X, Cao L, Su H (2016). Pedogenesis and physicochemical parameters influencing soil carbon and nitrogen of alpine meadows in permafrost regions in the northeastern Qinghai-Tibetan Plateau. Catena 141: 85-91.
CrossRef | Gscholar
(27)
Myers-Smith I (2011). Shrub encroachment in arctic and alpine tundra: mechanisms of expansion and ecosystem impacts. PhD thesis, University of Alberta, Alberta, Canada, pp. 142.
Online | Gscholar
(28)
Nachtergaele F, Velthuizen H, Verelst L, Wiberg D, Batjes N, Dijkshoorn K, Engelen V, Fischer G, Jones A, Montanarella L, Petri M, Prieler S, Teixeira E, Shi X (2012). Harmonized world soil database (version 1.2). FAO, Rome, Italy and IIASA, Laxenburg, Austria.
Gscholar
(29)
Naito AT, Cairns DM (2011). Patterns and processes of global shrub expansion. Progress in Physical Geography-Earth and Environment 35: 423-442.
CrossRef | Gscholar
(30)
Nie X, Xiong F, Yang L, Li C, Zhou G (2017). Soil nitrogen storage, distribution, and associated controlling factors in the northeast Tibetan Plateau shrublands. Forests 8 (11): 416.
CrossRef | Gscholar
(31)
Nie X, Yang L, Xiong F, Li C, Fan L, Zhou G (2018). Aboveground biomass of the alpine shrub ecosystems in Three-River Source Region of the Tibetan Plateau. Journal of Mountain Science 15: 357-363.
CrossRef | Gscholar
(32)
Nie X, Yang L, Li F, Xiong F, Li C, Zhou G (2019). Storage, patterns and controls of soil organic carbon in the alpine shrublands in the Three Rivers Source Region on the Qinghai-Tibetan Plateau. Catena 178: 154-162.
CrossRef | Gscholar
(33)
Obu J, Lantuit H, Myers-Smith I, Heim B, Wolter J, Fritz M (2017). Effect of terrain characteristics on soil organic carbon and total nitrogen stocks in soils of Herschel Island, western Canadian arctic. Permafrost and Periglacial Processes 28: 92-107.
CrossRef | Gscholar
(34)
Post WM, Pastor J, Zinke PJ, Stangenberger AG (1985). Global patterns of soil nitrogen storage. Nature 317: 613-616.
CrossRef | Gscholar
(35)
Qin D (2014). Eco-preservation and sustain development in the Three Rivers Source region of the Tibetan Plateau, China: responses to climate variability and human activities in the Three Rivers Source region mainly ecosystem. Science Press, Beijing, China, pp. 15-29.
Gscholar
(36)
R Development Core Team (2012). R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria.
Online | Gscholar
(37)
Tian H, Wang S, Liu J, Pan S, Chen H, Zhang C, Shi X (2006). Patterns of soil nitrogen storage in China. Global Biogeochemical Cycles 20 (1): GB1001.
CrossRef | Gscholar
(38)
Todd-Brown KEO, Randerson JT, Hopkins F, Arora V, Hajima T, Jones C, Shevliakova E, Tjiputra J, Volodin E, Wu T, Zhang Q, Allison SD (2014). Changes in soil organic carbon storage predicted by Earth system models during the 21st century. Biogeosciences 11: 2341-2356.
CrossRef | Gscholar
(39)
Vitousek PM, Farrington H (1997). Nutrient limitation and soil development: experimental test of a biogeochemical theory. Biogeochemistry 37: 63-75.
CrossRef | Gscholar
(40)
Wang S, Duan J, Xu G, Wang Y, Zhang Z, Rui Y, Luo C, Xu B, Zhu X, Chang X, Cui X, Niu H, Zhao X, Wang W (2012). Effects of warming and grazing on soil N availability, species composition, and ANPP in an alpine meadow. Ecology 93: 2365-2376.
CrossRef | Gscholar
(41)
Yang Y, Ma W, Mohammat A, Fang J (2007). Storage, patterns and controls of soil nitrogen in China. Pedosphere 17: 776-785.
CrossRef | Gscholar
(42)
Zhang X, Liu M, Zhao X, Li Y, Zhao W, Li A, Chen S, Chen S, Han X, Huang J (2018). Topography and grazing effects on storage of soil organic carbon and nitrogen in the northern China grasslands. Ecological Indicators 93: 45-53.
CrossRef | Gscholar
(43)
Zhao L, Wu X, Wang Z, Sheng Y, Fang H, Zhao Y, Hu G, Li W, Pang Q, Shi J, Mo B, Wang Q, Ruan X, Li X, Ding Y (2018). Soil organic carbon and total nitrogen pools in permafrost zones of the Qinghai-Tibetan Plateau. Scientific Reports 8 (1): 21.
CrossRef | Gscholar
(44)
Zhou Y, Boutton TW, Xu X (2018). Soil C:N:P stoichiometry responds to vegetation change from grassland to woodland. Biogeochemistry 140: 341-357.
CrossRef | Gscholar

Authors’ Affiliation

(1)
Xiuqing Nie 0000-0003-1543-9692
Dong Wang
Key Laboratory of Tree Breeding and Cultivation of the State Forestry Administration, Research Institute of Forestry Chinese Academy of Forestry, Beijing 100091 (China)
(2)
Xiuqing Nie 0000-0003-1543-9692
Dong Wang
Research Institute of Natural Protected Area, Chinese Academy of Forestry, Beijing 100091 (China)
(3)
Xiuqing Nie 0000-0003-1543-9692
Lucun Yang 0000-0003-3952-3039
Guoying Zhou 0000-0003-2485-6172
Key Laboratory of Tibetan Medicine Research, Northwest Institute of Plateau Biology, Chinese Academy of Science, Xining 810008 (China)
(4)
Lucun Yang 0000-0003-3952-3039
Guoying Zhou 0000-0003-2485-6172
Qinghai Key Laboratory of Qing-Tibet Biological Resources, Xining, 810008 (China)

Corresponding author

 
Guoying Zhou
zhougy@nwipb.cas.cn

Citation

Nie X, Wang D, Yang L, Zhou G (2020). Controlling soil total nitrogen factors across shrublands in the Three Rivers Source Region of the Tibetan Plateau. iForest 13: 559-565. - doi: 10.3832/ifor3533-013

Academic Editor

Giorgio Alberti

Paper history

Received: May 22, 2020
Accepted: Sep 20, 2020

First online: Nov 29, 2020
Publication Date: Dec 31, 2020
Publication Time: 2.33 months

© SISEF - The Italian Society of Silviculture and Forest Ecology 2020

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